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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594299Generated: October 31, 2026

Carbon tetrabromide → 5-(Bromomethyl)-2-(difluoromethoxy)pyridine

https://huagongshe.com/reaction/594299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(6-(Difluoromethoxy)pyridin-3-yl)methanolHCID 69085050—
SolventDichloromethaneHCID 6344—
Product5-(Bromomethyl)-2-(difluoromethoxy)pyridineHCID 69085387—

Reaction Steps

A solution of (6-(difluoromethoxy)pyridin-3-yl)methanol (246 mg; 1.41 mmol) in anh. DCM (10 ml) was treated at rt with CBr4 (467 mg; 1.41 mmol), and with triphenylphosphine (369 mg; 1.41 mmol). The resulting mixture was further stirred at rt, under nitrogen, for 15 h. Concentration to dryness under reduced pressure, and subsequent purification by FC (DCM) afforded 5-(bromomethyl)-2-(difluoromethoxy)pyridine as an orange oil 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-8c73e791e87745f0a7e9789d18ec12ae
Source noteuspto-grants-2016_01