Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179044Generated: November 2, 2026

Acetic Acid → HCID 10221947, compound

https://huagongshe.com/reaction/1179044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(+-)-alpha-MethyltryptamineHCID 9287—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 69337492HCID 69337492—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 10221947HCID 10221947152.4%

Reaction Steps

348 mg DL-α-methyltryptamine were dissolved in dry 1,2-dichloroethane (10 ml) under argon (clear solution), 463 mg 4-benzyl-4-dimethylamino-cyclohexane (see example 3) and glacial acetic acid (229 μl) were added and the mixture was stirred for one hour at RT. 550 mg sodium triacetoxyborohydride were then added and the suspension was stirred for a further 72 hours at RT. For working up, water (20 ml) was added to the reaction mixture, the organic phase was separated off and the aqueous phase was extracted once with ether and then rendered strongly alkaline with sodium hydroxide solution (pH>10). A gelatinous precipitate which dissolved in ethyl acetate thereby precipitated out. The aqueous phase was extracted with ethyl acetate (4×10 ml). All the ethyl acetate phases were combined, dried with sodium sulfate and concentrated to dryness. 766 mg of a mixture of cis- and trans-1-benzyl-N′-[2-(1H-indol-3-yl)-1-methylethyl]-N,N-dimethylcyclohexane-1,4-diamine were obtained as a vitreous solid (m.p. 48-53° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276518B2
Source datasetuspto-grants-2007_10
ORD IDord-9c5b0d5222b8422cba93b896a2901dc7
Source noteuspto-grants-2007_10