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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179042Generated: October 31, 2026

Benzoyl chloride → HCID 10155696, compound

https://huagongshe.com/reaction/1179042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 69337829HCID 69337829—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 10155696HCID 10155696—
ProductHCID 69337858HCID 69337858—

Reaction Steps

3.00 g 1-benzyl-N′-ethyl-N,N-dimethyl-cyclohexane-1,4-diamine were dissolved in 50 ml methylene chloride, and 1.68 ml triethylamine and approx. 10 mg DMAP were added. 1.40 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 (4.05 g) was chromatographed over silica gel with methanol/ether 1:1. 1.09 g of the polar diastereomer of N-(4-benzyl-4-dimethylamino-cyclohexyl)-N-ethyl-benzamide were obtained, from which 1.01 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-f6d6c5ea2a6e48149ae2a69e216a9f06
Source noteuspto-grants-2007_10