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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66810Generated: October 26, 2026

Ethyl chloroformate → N-(1-Methyldecyl)-3-(3-Nitrophenyl)-2-butenamide

https://huagongshe.com/reaction/66810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-UndecanamineHCID 114476—
Reactant3-(3-Nitrophenyl)-2-butenoic acidHCID 54402156—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-(1-Methyldecyl)-3-(3-Nitrophenyl)-2-butenamideHCID 53905448—

Reaction Steps

To a stirred slurry of 5.2 g. of the 3-(3-nitrophenyl)-2-butenoic acid from Preparation 12 having a melting point of 208°-210° C., in 100 ml. of dichloromethane, was added 2.8 g. of triethylamine in 10 ml. of dichloromethane. This was followed by the addition of a solution of 3.0 g. of ethyl chloroformate in 20 ml. of dichloromethane, during 20 minutes. Stirring was continued for 30 minutes, and then a solution of 1-methyldecylamine in 20 ml. of dichloromethane was added dropwise during 25 minutes. Stirring was continued overnight, and the the reaction mixture was washed successively with 1 N potassium carbonate, water and saturated sodium chloride. The resulting solution was dried using sodium sulfate, and then it was evaporated in vacuo leaving an oil which solidified on trituration under petroleum ether. This afforded 4.9 g. of the title compound, m.p. 72.5°-74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04343813
Source datasetuspto-grants-1982_08
ORD IDord-921caf7094484586aeaa6606fc5056d7
Source noteuspto-grants-1982_08