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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415646Generated: October 26, 2026

Bromoacetyl bromide → N-(4-n-butyl-2-nitrophenyl)-2-bromoacetamide

https://huagongshe.com/reaction/1415646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantBenzenamine, 4-butyl-2-nitro-HCID 77229—
SolventTolueneHCID 1140—
ProductN-(4-n-butyl-2-nitrophenyl)-2-bromoacetamideHCID 2148299586.8%

Reaction Steps

A solution of 4-n-butyl-2-nitroaniline (29.1 g) in toluene (100 ml) was treated with bromoacetyl bromide (33.3 g). The mixture was boiled under reflux for 3/4 hour and the toluene evaporated off. The residual oil was poured into petroleum spirit (b.p. 60°-80° C; 400 ml). Crystals were deposited and these were removed by filtration to give N-(4-n-butyl-2-nitrophenyl)-2-bromoacetamide (41 g), m.p. 56°-57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005217
Source datasetuspto-grants-1977_01
ORD IDord-34f540d0d41d41dbb854a8055330ba82
Source noteuspto-grants-1977_01