Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594308Generated: November 2, 2026

Carbon tetrabromide → 2-(Bromomethyl)-4-(difluoromethoxy)pyridine

https://huagongshe.com/reaction/594308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-(Difluoromethoxy)pyridin-2-yl)methanolHCID 69082615—
SolventDichloromethaneHCID 6344—
Product2-(Bromomethyl)-4-(difluoromethoxy)pyridineHCID 69080160—

Reaction Steps

A solution of (4-(difluoromethoxy)pyridin-2-yl)methanol (250 mg; 1.42 mmol) in anh. DCM (12 ml) was treated at rt with CBr4 (473 mg; 1.42 mmol), and with PPh3 (374 mg; 1.42 mmol). The resulting mixture was further stirred at rt, under nitrogen, for 1 h. Concentration to dryness under reduced pressure, and subsequent purification by FC (DCM) afforded 2-(bromomethyl)-4-(difluoromethoxy)pyridine as a yellow oil which was directly used for the next reaction. LC-MS (conditions A): tR=0.56 min.; [M+H]+: 237.92 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-23b028bf89f54aabae123c67689ba62e
Source noteuspto-grants-2016_01