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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594315Generated: November 1, 2026

Carbon tetrabromide → 2-(Bromomethyl)-1-benzofuran

https://huagongshe.com/reaction/594315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant1-Benzofuran-2-YlmethanolHCID 2776263—
SolventDichloromethaneHCID 6344—
Product2-(Bromomethyl)-1-benzofuranHCID 12326316—

Reaction Steps

A solution of benzofuran-2-ylmethanol (120 mg; 0.81 mmol) in anh. DCM (5 ml) was treated at rt with CBr4 (268 mg; 0.81 mmol), and with PPh3 (212 mg; 0.81 mmol). The resulting mixture was further stirred at rt, under nitrogen, for 17 h. Concentration to dryness under reduced pressure, and subsequent purification by FC (DCM) afforded 2-(bromomethyl)benzofuran as a yellow oil (128 mg; 75%) which was directly used for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-d9a89dc8e5b345cd95202de71e5886a7
Source noteuspto-grants-2016_01