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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278787Generated: October 29, 2026

Triphenylphosphine → 4-Bromo-1-(bromomethyl)-2-methylbenzene

https://huagongshe.com/reaction/278787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant(4-Bromo-2-methylphenyl)methanolHCID 22280088—
SolventDichloromethaneHCID 6344—
Product4-Bromo-1-(bromomethyl)-2-methylbenzeneHCID 22569018—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (4-bromo-2-methyl-phenyl)-methanol (Intermediate 133, 319.0 mg, 1.58 mmol) and triphenylphosphine (466.0 mg, 1.74 mmol) in 5 mL CH2Cl2 was cooled to 0° C. and N-bromosuccinimide (309.0 mg, 1.74 mmol) was added in 5 portions over 20 minutes. The solution was warmed to 25° C. and stirred for 17 hours. The reaction was quenched by the addition of dilute aqueous NaHCO3. The resulting mixture was extracted with Et2O and the combined organic layers were washed with H2O and saturated aqueous NaCl before being dried (Na2SO4) and concentrated under reduced pressure. The title compound, 350.0 mg (84%), was isolated by column chromatography (2-3% EtOAc-hexanes) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359135B1
Source datasetuspto-grants-2002_03
ORD IDord-7a210ad77d2e4119801efe2488364269
Source noteuspto-grants-2002_03