Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599073Generated: November 2, 2026

Triethylamine → 2-Bromo-N-isopropyl-N-(4-methoxyphenyl)acetamide

https://huagongshe.com/reaction/1599073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
Reactant4-methoxy-N-(propan-2-yl)anilineHCID 2759498—
SolventDichloromethaneHCID 6344—
Product2-Bromo-N-isopropyl-N-(4-methoxyphenyl)acetamideHCID 1077953494.1%

Reaction Steps

To a solution of isopropyl-(4-methoxyphenyl)-amine (25.11 g, 152 mmol) in dichloromethane (250 mL) was added triethylamine (15.38 g, 152 mmol) with stirring at ambient temperature. The solution was cooled in an ice bath (<3° C.) and bromoacetyl bromide (30.68 g, 152 mmol) dissolved in dichloromethane (100 mL) was added dropwise over a 45 minute period. The reaction mixture was stirred overnight at ambient temperature, washed with 0.3N HCl (300 mL) and brine (300 mL), dried over sodium sulfate, filtered, and evaporated under reduced pressure to give a dark brown oil. The oil was filtered through a pad of silica gel (150 g) which was eluted with ethyl acetate/hexane (1:1, 900 mL) and the filtrate evaporated under reduced pressure to afford the title compound (41.05 g, 143 mmol) as a brown oil which crystallized on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739129
Source datasetuspto-grants-1998_04
ORD IDord-4b65292db6b541f3a6aa91ed4f2f5222
Source noteuspto-grants-1998_04