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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308571Generated: November 1, 2026

Hydrochloric Acid → HCID 12723322, compound

https://huagongshe.com/reaction/2308571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnilineHCID 6115—
ReactantN,N-DiethylanilineHCID 7061—
Reactant2-Bromoprop-2-enoyl chlorideHCID 18418029—
SolventDichloromethaneHCID 6344—
ProductHCID 12723322HCID 1272332265.5%

Reaction Steps

A vigorously stirred solution of 4.5 grams (0.027 mole) of 2-bromopropenoyl chloride (Step B product) in 150 ml of dried methylene chloride was cooled to 5°±5°. To this was added dropwise 4.0 grams (0.027 mole) of N,N-diethylaniline at such a rate that the reaction mixture temperature did not exceed 10°. Upon completion of addition, 2.5 grams (0.027 mole) of aniline was added dropwise while continuing to maintain the reaction mixture temperature below 10°. The reaction mixture was allowed to warm to ambient temperature where it was stirred for two hours. After dilution with 100 ml of aqueous 1N hydrochloric acid, the reaction mixture was poured into a separatory funnel. The organic layer was separated and extracted with 50 ml of aqueous 1N hydrochloric acid, then with 100 ml of an aqueous solution saturated with sodium bicarbonate. The organic layer was dried with magnesium sulfate. The mixture was filtered and the filtrate concentrated under reduced pressure to a residual solid. The solid was dissolved in methylene chloride and decolorized with silica gel. The mixture was filtered and the filtrate concentrated under reduced pressure to a residual solid. The solid was recrystallized from hexane to give 4.0 grams of 2-bromo-N-phenyl-2-propenamide; mp 90.5°-92.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSH0000327
Source datasetuspto-grants-1987_09
ORD IDord-487d02a6e6664130a6d2a3d2b8331585
Source noteuspto-grants-1987_09