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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167612Generated: October 31, 2026

Triphenylphosphine → 1-(2-Bromo-ethoxymethyl)-4-chlorobenzene

https://huagongshe.com/reaction/2167612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant2-[(4-Chlorobenzyl)oxy]-1-ethanolHCID 2763751—
SolventDichloromethaneHCID 6344—
SolventAluminumHCID 5359268—
Product1-(2-Bromo-ethoxymethyl)-4-chlorobenzeneHCID 1365437457%

Reaction Steps

A solution of N-bromosuccinimide (272 mg, 1.53 mmol) in DCM (2.5 mL) was added to resin-bound triphenylphosphine (510 mg, 1.53 mEquiv, Fluka) in DCM (2.5 mL), and the reaction was stirred at rt for 10 min. A solution of 2-{[(4-chlorophenyl)methyl]oxy}ethanol (129 mg, 0.691 mmol) in DCM (1.5 mL) was added to the reaction, and the residual alcohol was transferred with additional DCM (1.5 mL). The reaction vial was capped, wrapped in aluminum foil, and stirred at rt for 20 h. The reaction was filtered through a SPE cartridge (5 g silica) eluting with the following 10 mL fractions: DCM (fraction 1), 30% EtOAc/hexanes (fraction 2), and 50% EtOAc/hexanes (fraction 3) to give the title compound (98 mg, 57%). The product was characterized by 1H NMR (400 MHz) in CDCl3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045469B2
Source datasetuspto-grants-2015_06
ORD IDord-e8e3b6d07cbb41e5ab70cb7b19936573
Source noteuspto-grants-2015_06