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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704592Generated: October 30, 2026

Triethylamine → HCID 15101124, compound

https://huagongshe.com/reaction/704592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-Phenethylamine, (-)-HCID 75818—
Reactant2-(4-oxocyclohexyl)acetic AcidHCID 9920438—
SolventDichloromethaneHCID 6344—
ProductHCID 15101124HCID 15101124143.2%

Reaction Steps

A solution of 4-oxocyclohexaneacetic acid (28.39 g) (Example H) and triethylamine (30.4 ml) in 800 ml of dichloromethane at -10° C. is treated dropwise with isobutyl chloroformate (26.0 ml). The reaction mixture is stirred at this temperature for 15 minutes and 1(S)-phenylethylamine (26.51 g) is added via syringe. After 30 minutes at -10° C., the mixture is stirred at room temperature for another 30 minutes. The reaction is concentrated in vacuo and the residue partitioned between ethyl acetate (1000 ml) and 1 N hydrochloric acid solution (400 ml). The organic extract is washed with 1 N sodium hydroxide solution and brine, dried (magnesium sulfate), and concentrated in vacuo to leave 67.5 g of crude (S)-4-oxo-N-(1-phenylethyl)cyclohexaneacetamide as a white solid; mp 110°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988699
Source datasetuspto-grants-1991_01
ORD IDord-53f90297b01344a3ac10c331ebf78d36
Source noteuspto-grants-1991_01