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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844782Generated: October 31, 2026

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

https://huagongshe.com/reaction/844782

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 numberUS06380256B1
Source datasetuspto-grants-2002_04
ORD IDord-f40b5c035a064092a6a34fc876d856fd
Source noteuspto-grants-2002_04