----DissoSilver----
over the last couple years i have compiled and analyzed most of the information you will need to attempt such a task. if anyone attempts the feat please private message me? it requires some basic chemistry reaction knowledge but you can look up most of the reactions for a basic explanation as well as use the ketamine production instructions i have listed for specifics on what to do at each step (you will have to work out which steps to skip based on using the precursor i have listed). if someone wants to look at all the equipment you would need and add it to this thread i would gladly add it to the recipe. here's what i got.

"It's a four step grignard reaction from the precursors which are easy to obtain and it follows the ketamine synthesis procedure. It's 11 steps from scratch which includes preparing your grignard reagents if not using precursor shortcuts."

                               ----simplified Synthesis MXE (using precursor)----
to see the exact specifics on what to do see the ketamine synthesis and extrapolate what actions to take with the precursors etc.

                               ----1.) begin with a cyclopentyl gridnard using-

                      -cyclopentyl bromide      -magnesium        -Diethyl ether

                               ----2.)then react with-

                3-methoxybenzonitrile (use as precursor shortcut unless you can make this yourself)

                               which forms - (3-methoxyphenyl cyclopentyl ketone)

                               ----3.)brominate alpha using (ketone halogenation)

                      The reaction may be carried out under either acidic or basic conditions
                         in an aqueous medium with the corresponding elemental halogen

                               ----4.)convert the alpha-bromo ketone to schiff base with ethylamine

                               ----5.)Heat base synthesized ketone forming Methoxetamine.

                               ----6.)optional, dissolve impurities with acetone.

                                     ----synthesis explained MXE:----
Methoxetamine is synthesized utilizing an analogous procedure for that of ketamine. A cyclopentyl Grignard was reacted with 3-methoxybenzonitrile to form 3-methoxyphenyl cyclopentyl ketone, which was then brominated alpha to the ketone. The alpha-bromo ketone was converted to the Schiff’s base with ethyl amine, which was then heated to form methoxetamine.

A significant amount of a by-product (impurity) was produced during the synthesis of methoxetamine. The impurity was easily isolated from methoxetamine HCl by its solubility in acetone.

                                         ----synthesis addition----
Synthesis The World Health Organization released a thorough review of Methoxetamine in 2014 including detailed chemistry data.‘The synthesis of methoxetamine was achieved by 4 steps through simple reactions involving an aromatic nitrile, a Grignard reagent, bromination, imine formation through reaction with a suitable amine, followed by the application of heat to the product to allow ring expansion of 1­[(ethylimino)(3­ methoxyphenyl)methyl]­1­cyclopentanol [2]. This process is presumably readily applicable to analogues of methoxetamine by substitution of starting aromatic nitrile and selected amine to afford the desired N­substituted derivative analogues of methoxetamine [3].’ [http://www.who.int/medicines/areas/quality_safety/4_22_review.pdf]. Additional synthesis information can be found in the US Drug Enforcement Agency’s Microgram journal article The Characterization of 2­(3­Methoxyphenyl)­2­(ethylamino)cyclohexanone (Methoxetamine). Stereochemistry

Similar to ketamine, there exists 2 MXE isomers, ‘S’ and ‘R’. The vast majority of available MXE has been racemic, which means there is an equal ratio of S to R. These isomers also apply to ketamine. S ketamine is more highly sought after than R for it produces a notably stronger and more psychedelic experience, so it is not surprising that S­MXE produces a stronger and often preferred experience to racemic.

                                         ----KETAMINE SYNTHESIS FULL----
Experimental

o-Chlorobenzoic acid Anthranilic acid 13,7g HCl (conc., d=1,19) NaNO2 8g CuCl 10g
13,7g anthranilic acid is stirred in a glass beaker in 40mls water, 28mls HCl and 20g ice. With constant stirring and cooling there's added 8g NaNO2 in 40mls water. Thus obtained clear solution of diazonium salt is very slowly added with stirring into a soln. of 10g CuCl in 25g HCl conc. A vigorous evolution of nitrogen is observed. When the rxn ends, the ppt is filtered, washed with cold water and reprecipitated from aq. Na2CO3. The product represents fine crystals and melts at 140-141°C. o-Bromobenzoic acid can bee obtained in an analogous manner, substituting CuCl for CuBr.

o-Chlorobenzonitrile
Preparation A.

(RCOO)2Zn + Pb(SCN)2 = 2 RCN + ZnS + PbS + 2 CO2 The best results are obtained when a zinc salt is employed instead of free acid. This rxn is unsuitable for amino-, nitro- and oxy- acids, but can bee used for bromo- and chlorobenzoic acids. To a hot soln of 50g NaOH in 400mls water there's added 195g o-chlorobenzoic acid. Carefully neutralize with NH3 or NaHCO3 and add with heating 105g (~5% excess) ZnSO4 in 400mls water. The precipitated salt is dried for prolonged time at 200°C and mixed intimately with 205g Pb(SCN)2. The mixture is coffeeground and dried at 120-140°C for a prolonged time, then heated on open flame - the mixture melts and gases are evolved. Distilled nitrile is treated with NH4OH, steam-distilled and salted out. Yield 137g (80%), mp 43-46°C, bp 232°C. The rxn usually takes place within 30-60 mins, but the duration of dryings makes the method quite time-consuming.

Preparation B.

This one doesn't require a prolonged drying. Sulfaminic acid is dirt cheap and can bee acquired without causing any suspicion. o-Bromobenzonitrile 50g o-Bromobenzamide and 35g (25g=theory) sulfaminic (sulfamic) acid is thoroughly mixed and heated in a Wurtz flask. At 250-255°C distillation begins, which is over at 285-295°C (takes approx. 1.5-2 hrs). The collected product is redistilled, yield 36g (80% of theory). mp 53-57°C, bp 251-253°C As I found recently, this can bee simplified yet more, by forming benzamides in situ from the corresponding acid and urea..but since this is a very good route to subst’d benzaldehydes from benzoic acids, I’ll post it later separately.

Cyclopentanone
100g adipic acid and 10g Ba(OH)2 is intimately mixed and placed into a flask with a thermometer. The rxn is heated to 280°C, the mixture initially melts and then the distillation takes place, which lasts about 1-2 hrs. The hot distillate is saturated with NaCl, the upper layer is decanted and distilled, collecting the fraction boiling at 128-130°C. Dry with MgSO4. Yield: 51g (89% of theory). Notes: Ca(OH)2 may bee substituted for Ba(OH)2 without much loss in the yield. if one is to use pre-made Ca or Ba adipinate, no temp control is necessary.

Aluminium isopropoxide
Al(i-PrO)3 - Bp 130-140°C at 7mmHg; mp 118°C. Into a 250ml RBF equipped with an efficient reflux condenser there's added 6g Al foil, 70mls (51mls in theory) abs. IPA (commercial reagent grade IPA was used without any drying) and 0,1g HgSO4. The mixture is heated. In the beginning of boiling 0,5mls CCl4 (CAREFUL! Extremely toxic!) and heating continued until H2 evolution starts, when it is stopped, sometimes even cooling's needed. After the rxn subsides, heating is continued until almost full dissolution of Al (5-7 hrs). The obtained solution is immediately used as is in the following preparation.

Cyclopentanol
Into a 250ml RBF equipped with a 15cm Vigreux column and distilling condenser there's added 53mls (50g) cyclopentanone in 50mls IPA and the soln from the previous prep'n, which contains about 40g Al isopropoxide. The rxn is gently heated, which causes acetone with some water to distill off. The distillation is ended when the temp of the vapors rises to ~85°C. The ppt inside the flask is carefully decomposed with 50% H2SO4 until acidic and saturated with NaCl. The upper layer is decanted and distilled, collecting the fraction boiling at 137-140°C. Drying with MgSO4. Yield: 47g (94%)

Cyclopentylbromide
In a flask there’s mixed 47mls (45g) cyclopentanol and 60mls (90g) 48% aq. HBr. 10g Na2SO4 is added. The rxn is left for 24hrs with vigorous stirring. After that it’s diluted with 200mls water and the lower organic phase is separated and washed with water twice. Distill, collecting the fraction between 137-138°C. Dryed with MgSO4. Yield = 58g (74%)

Cyclopentyl magnesium bromide
Into a 250mls three-necked flask equipped with a reflux condenser, addition funnel and inert gas inlet there’s placed 50mls THF (kept over KOH, prior to the rxn 150mls refluxed over 30g CaO for 6hrs and distilled). 9g of fine Mg turnings is added followed by some iodine crystals. The apparatus is flushed with argon and a gentle stream of gas is left flowing in. Magnetic stirring is commenced. The mixture instantly beecomes cloudy from MgI. From the addition funnel there’s dripped 55g (40mls) cyclopentyl bromide in 100mls THF so that the soln boils smoothly. The rxn is usually over in an hour, it is accompanied by precipitation of a white jelly-like mass, and at the bottom there maybee left some unreacted Mg as a dark-grey powder. Usage of THF instead of ether is preferred since the rxn in it proceeds better and faster (THF is a more specific solvent for Grignards) , the yield is better as well. Beesides, THF can bee dried with CaO, while for ether,sodium metal is usually employed. Notes on the possible usage of Zn-organics: ".. Nitriles are not bad as electrophiles, so it is possible that despite smaller reactivity of ZnR2 compounds, they would work equally well here - esp. if the rxn conditions are made harsher (gentle reflux instead of RT?). What one CAN say for sure-is that the rxn with ZnR2 will go just fine if one is to use o-chlorobenzoyl chloride instead of benzonitrile. Haloanhydrides generally are the best species for coupling with metalloorganics. Bis-dicyclopentyl zinc is conveniently made from the corresponding bromide, no need to make iodide here. And o-chlorobenzoyl chloride can bee easily prepared from o-chlorobenzoic acid (obtained in Step 1) and PCl5 or some such."

o-Chlorophenyl cyclopentyl ketone
To the thus obtained Grignard soln there’s added 48g o-chlorobenzonitrile and the mixture is stirred for 3 days at RT. It is then poured into a mixture of ice/NH4Cl, with addition of some conc. aq. NH3 and left at ambient temp until all ice melts. The ketone partially floats, partially goes to the bottom. It’s extracted with benzene. The yields fluctuate, but rarely drop beelow 55%.

alpha-Bromo-(o-chlorophenyl)-cyclopentyl ketone
40g ketone is dissolved in 70mls CCl4 and with cooling in snow it is added into a soln of 48g dioxane dibromide in 50mls dioxane, and stirred at RT for 30mins. Then 30mls water are added and the soln is washed with Na2CO3 aq. until neutral. This may lead to some preciptation of the bromoketone, which stays in CCl4. The solvent is removed, giving 47g (85%) of the bromoketone.

(1-hydroxy-cyclopentyl)-(o-chlorophenyl)-N-methylketimine
45g of the above bromoketone is dissolved in 50mls benzene, add therein 50mls triethylamine (17g/23mL is required for neutralization of HBr, but a 2x excess is used). The soln is then saturated with 5g methylamine, obtained by dripping a saturated soln of 15g MeNH2·HCl onto 10g NaOH, dried thru NaOH. The rxn is left for 1 day and the solvents are removed under aspirator vacuum, giving 30g (80%) of methylketimine.

Ketamine
10g of methylketimine is dissolved in 100mls undecane and boiled at 195°C for 3-4hrs. Ketamine is extracted with 20% HCl. Acidic extract is basified and extracted with DCM. Solvent is removed giving the product as an oil that quickly crystallizes. It can bee purified by recrystallization from pentane/ether or hexane/ether. The yields are close to quantitative.