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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483749Generated: October 29, 2026

N-bromobutanimide → (2RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-[(RS)-alpha-bromo-3-phenoxybenzyloxy]-propane

https://huagongshe.com/reaction/483749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-(4-Ethoxyphenyl)-3,3,3-trifluoropropyl 3-phenoxybenzyl etherHCID 10669581—
SolventCarbon TetrachlorideHCID 5943—
Product(2RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-[(RS)-alpha-bromo-3-phenoxybenzyloxy]-propaneHCID 19753527—

Reaction Conditions

Temperature0 °C

Reaction Steps

A catalytic amount of α,α'-azo-iso-butyronitrile was added to a solution of N-bromosuccinimide (0.14 g) and (RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-(3-phenoxybenzyloxy)propane (0.3 g) in carbon tetrachloride (14 cm3). The reaction mixture was heated at the reflux temperature for 90 minutes, then cooled to 0° C., filtered, and the filtrate concentrated by evaporation under reduced pressure to leave (2RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-[(RS)-α-bromo-3-phenoxybenzyloxy]-propane as a pale yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225607
Source datasetuspto-grants-1993_07
ORD IDord-079204e5cf5f4cfd9c130bd3f8a24d46
Source noteuspto-grants-1993_07