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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373735Generated: October 31, 2026

N,N-Dimethylaniline → N-[4-benzyloxy-2,6-bis(trifluoromethyl)phenyl]-2-bromoacetamide

https://huagongshe.com/reaction/1373735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantBromoacetyl bromideHCID 61147—
Reactant4-Benzyloxy-2,6-bis(trifluoromethyl)anilineHCID 21075600—
SolventTolueneHCID 1140—
ProductN-[4-benzyloxy-2,6-bis(trifluoromethyl)phenyl]-2-bromoacetamideHCID 2107560364.7%

Reaction Steps

Under an argon atmosphere, N,N-dimethylaniline (2.78 mL, 21.9 mmol) and bromoacetyl bromide (1.91 mL, 21.9 mmol) were added dropwise to a solution of 4-benzyloxy-2,6-bis(trifluoromethyl)aniline (4.90 g, 14.6 mmol) in anhydrous toluene (150 mL) under ice cooling. Immediately after the dropwise addition, the mixture was heated under reflux and then stirred for 1 hour. After cooling, the reaction mixture was filtered through Celite and the insoluble matter was washed with toluene. The residue obtained by distilling the filtrate under reduced pressure was purified by chromatography on a silica gel column (developing solvent; hexane:acetone=10:1→6:1→5:1). The crude product thus obtained was recrystallized from hexane-acetone, whereby 4.31 g (yield: 64.7%) of N-[4-benzyloxy-2,6-bis(trifluoromethyl)phenyl]-2-bromoacetamide was obtained as colorless needle-like crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163944B2
Source datasetuspto-grants-2007_01
ORD IDord-758d94ad5a20437e9bbeb57198c2ac0d
Source noteuspto-grants-2007_01