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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441560Generated: October 30, 2026

Hydrochloric Acid → 3-(3-bromophenyl)-N-ethylprop-2-enamide

https://huagongshe.com/reaction/441560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylamineHCID 6341—
ReactantEthyl 3-(3-bromophenyl)acrylateHCID 5369361—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product3-(3-bromophenyl)-N-ethylprop-2-enamideHCID 42754—

Reaction Conditions

Temperature45 °C

Reaction Steps

Trans ethyl 3-bromocinnamate (8.4 g), ethylamine (6.7 g), methanol (18 ml) and 4A molecular sieves (1 g) were combined and heated at reflux for 1/2 hour. The mixture was cooled to about 45° C. and sodium methylate (0.6 g) added. The mixture was then heated at reflux 11/2 hour and then cooled. It was acidified with concentrated hydrochloric acid (12 ml). The sieves were removed by filtration. Ice water was added to the filtrate to precipitate trans 3-bromo-N-ethylcinnamamide, m.p. 89°-90° C. (after recrystallization from ethanol/water).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04041071
Source datasetuspto-grants-1977_08
ORD IDord-ce7df936a4914e7a9cceb8701663e7c0
Source noteuspto-grants-1977_08