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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179066Generated: November 3, 2026

Acetic Acid → HCID 9924406, compound

https://huagongshe.com/reaction/1179066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1H-Indol-3-YlmethanamineHCID 472107—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9924406HCID 9924406—

Reaction Steps

970 mg C-(1H-Indol-3-yl)methylamine and 1.44 mg 4-dimethylamino-4-phenyl-cyclohexanone were dissolved in dry tetrahydrofuran (15 ml) and 1,2-dichloroethane (50 ml) under argon. Glacial acetic acid (13.2 mmol) and 1.82 g sodium triacetoxyborohydride were added to this mixture and the mixture was stirred for 72 hours at RT. For working up, the reaction mixture was concentrated, water (20 ml) and ether (30 ml) were added to the residue and the mixture was stirred vigorously. The aqueous phase was separated off, washed with ether (2×15 ml), adjusted to pH 11 with five molar sodium hydroxide solution and extracted with ethyl acetate (4×25 ml). The combined extracts were dried over sodium sulfate and filtered and the filtrate was concentrated. The crude product (2.11 g) was chromatographed over silica gel with methanol/triethylamine (199:1). 465 mg of the nonpolar diastereomer of N′-(1H-indol-3-ylmethyl)-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine were obtained (m.p. 182-184° C.), from which the corresponding dihydrochloride was precipitated with chlorotrimethylsilane (443 μl) in 2-butanone/acetone (20 ml/50 ml) (498 mg; m.p. 164-168° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276518B2
Source datasetuspto-grants-2007_10
ORD IDord-9ee5d885e9cb4e1babdce40498e93294
Source noteuspto-grants-2007_10