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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283114Generated: November 1, 2026

Triphenylphosphine → 1-{[(2-Bromoethyl)oxy]methyl}-4-(1,1-dimethylethyl)benzene

https://huagongshe.com/reaction/2283114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant2-({[4-(1,1-Dimethylethyl)phenyl]methyl}oxy)ethanolHCID 10488591—
SolventDichloromethaneHCID 6344—
SolventAluminumHCID 5359268—
Product1-{[(2-Bromoethyl)oxy]methyl}-4-(1,1-dimethylethyl)benzeneHCID 1365437812%

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-(1,1-dimethylethyl)phenyl]methyl}oxy)ethanol (160 mg, 0.768 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 (25 mg, 12%). The product was characterized by 1H NMR (400 MHz) in CDCl3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09144571B2
Source datasetuspto-grants-2015_09
ORD IDord-a807380dfb194efca361db0383eba373
Source noteuspto-grants-2015_09