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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66620Generated: October 25, 2026

Ethyl chloroformate → N-(1-Methyldecyl)-3-phenyl-3-(4-nitrophenyl)propenamide

https://huagongshe.com/reaction/66620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-UndecanamineHCID 114476—
Reactant3-(4-Nitrophenyl)-3-phenylprop-2-enoic acidHCID 53427600—
ProductN-(1-Methyldecyl)-3-phenyl-3-(4-nitrophenyl)propenamideHCID 5383662551%

Reaction Steps

The title compound was prepared from 3-phenyl-3-(4-nitrophenyl)propenoic acid via mixed anhydride formation using ethyl chloroformate, followed by reaction with 1-methyldecylamine, substantially according to the procedure of Preparation 21. The product was induced to solidify by trituration under hexane. The solid was recrystallized from hexane, giving a small amount of material which was discarded. The mother liquors were evaporated in vacuo to give an oil which solidified when stirred under acetonitrile. The solid was filtered off, giving a 51% yield of the title compound, m.p. 69°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342781
Source datasetuspto-grants-1982_08
ORD IDord-ca363b7f65534cd6b1c78e535ccde923
Source noteuspto-grants-1982_08