Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577472Generated: November 3, 2026

Benzene → N-(1-phenylcyclopropyl)-alpha-bromo-tert-butylacetamide

https://huagongshe.com/reaction/1577472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant1-Phenyl-cyclopropylamineHCID 194549—
Reactant2-Bromo-3,3-dimethylbutanoyl chlorideHCID 10867621—
SolventTriethylamineHCID 8471—
ProductN-(1-phenylcyclopropyl)-alpha-bromo-tert-butylacetamideHCID 1276053571.4%

Reaction Steps

Into a 200 ml four-necked flask, there were charged benzene (100 ml), 1-phenylcyclopropylamine (8.9 g) and triethylamine (7.4 g), and α-bromo-tert-butylacetyl chloride (14.5 g) was dropwise added thereto while stirring at room temperature. Stirring was continued for 3 hours. After completion of the reaction, the reaction mixture was washed with water to remove triethylamine hydrochloride. The benzene layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was recrystallized from ethanol to give 14.8 g of N-(1-phenylcyclopropyl)-α-bromo-tert-butylacetamide. M.P., 161°-162.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04288244
Source datasetuspto-grants-1981_09
ORD IDord-a7189525640c4b379108d7190376d22a
Source noteuspto-grants-1981_09