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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179040Generated: October 30, 2026

Benzoyl chloride → HCID 10132608, compound

https://huagongshe.com/reaction/1179040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 69338491HCID 69338491—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 10132608HCID 10132608—
ProductHCID 69336941HCID 69336941—

Reaction Steps

3.00 g 1-benzyl-N,N,N′-trimethyl-cyclohexane-1,4-diamine were dissolved in 50 ml methylene chloride, and 1.78 ml triethylamine and approx. 10 mg DMAP were added. 1.41 ml benzoyl chloride were added dropwise, while cooling in an ice/methanol bath, and the reaction mixture was then stirred overnight, while warming to room temperature. For working up, 50 ml five molar KOH solution and 50 ml water were added, the mixture was stirred for ten minutes and extracted three times with 50 ml methylene chloride each time, the combined extracts were dried over magnesium sulfate and filtered and the filtrate was concentrated. The crude product obtained (3.61 g) was chromatographed over silica gel with methanol/ether 1:1. 231 mg of the polar diastereomer of N-(4-benzyl-4-dimethylamino-cyclohexyl)-N-methyl-benzamide were obtained, from which 188 mg of the corresponding hydrochloride were prepared as described for example 1 with water and chlorotrimethylsilane in 2-butanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276518B2
Source datasetuspto-grants-2007_10
ORD IDord-887a448d8ba64fd28c3612783f3fe1d2
Source noteuspto-grants-2007_10