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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179086Generated: November 2, 2026

Acetic Acid → HCID 69337530, compound

https://huagongshe.com/reaction/1179086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantSodium SulfateHCID 24436—
ReactantL-Tryptophan, methyl esterHCID 77980—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 69337530HCID 69337530—

Reaction Steps

The hydrochloride of L-tryptophan methyl ester (1.01 g) was stirred vigorously for 15 minutes with 1,2-dichloroethane (20 ml) and saturated NaHCO3 solution (20 ml) and the aqueous phase was immediately extracted with 1,2-dichloroethane (2×20 ml). After drying with Na2SO4, the organic phase was concentrated to 40 ml, and 4-dimethylamino-4-phenylcyclohexanone (893 mg, 4 mmol.) was added thereto under argon. Glacial acetic acid (0.228 ml, 4 mmol.) and Na2SO4 (2 g) were added to the clear solution. After a reaction time of 15 minutes, NaBH(OAc)3 (1.2 g) was added to the reaction mixture, and stirring was carried out for 4 days at room temperature. For working up, saturated NaHCO3 solution (40 ml) was added and stirring was carried out for 15 minutes. The aqueous phase was extracted with dichloromethane (2×20 ml). The combined organic phases were dried and then concentrated, yielding a light-brown oil. Purification by column chromatography was carried out with ethyl acetate and methanol. The nonpolar diastereomer (918 mg; m.p. 108-112° C.) was dissolved in 2-butanone (15 ml) and converted with chlorotrimethylsilane (0.4 ml) into the corresponding dihydrochloride (white solid; 326 mg; m.p. 197-202° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276518B2
Source datasetuspto-grants-2007_10
ORD IDord-a9e8a77ef15e40a88a90419bc7c731b6
Source noteuspto-grants-2007_10