Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179062Generated: October 30, 2026

1,2-Dichloroethane → HCID 178482560, compound

https://huagongshe.com/reaction/1179062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
ReactantHCID 178507366HCID 178507366—
ProductHCID 178482560HCID 178482560—
ProductHCID 178482561HCID 178482561—

Reaction Steps

268 mg 5-Aminobenzotriazole and 435 mg 4-dimethylamino-4-phenyl-cyclohexanone were dissolved in dry 1,2-dichloroethane (20 ml) under argon. Glacial acetic acid (2 mmol) and 600 mg sodium triacetoxyborohydride were added to this mixture and the mixture was stirred for 24 hours at RT. For working up, the reaction mixture was concentrated and the residue was adjusted to pH 11 with five molar sodium hydroxide solution. The alkaline phase was diluted with water (10 ml) and extracted with ethyl acetate (3×20 ml). The combined extracts were dried over sodium sulfate and filtered and the filtrate was concentrated. The crude product was chromatographed over silica gel with ethyl acetate/ethanol (1:1). 135 mg of the nonpolar diastereomer of N′-(3H-benzotriazol-5-yl)-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine were obtained as a white solid, from which the corresponding hydrochloride was precipitated with 1.85 M ethanolic hydrochloric acid (0.54 ml) in 2-butanone (5 ml) (98 mg; m.p. 168-173° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276518B2
Source datasetuspto-grants-2007_10
ORD IDord-3a976a979e4e420caf5ffae903c52a7d
Source noteuspto-grants-2007_10