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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594301Generated: October 30, 2026

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

https://huagongshe.com/reaction/594301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(2-(Difluoromethoxy)pyridin-4-yl)methanolHCID 67032008—
SolventDichloromethaneHCID 6344—
Product4-(Bromomethyl)-2-(difluoromethoxy)pyridineHCID 69082503—

Reaction Steps

A solution of (2-(difluoromethoxy)pyridin-4-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 4-(bromomethyl)-2-(difluoromethoxy)pyridine as a yellow oil which was directly used for the next reaction. LC-MS (conditions A): tR=0.78 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-9fa2bb710cb1473db596aa723f0f6f8d
Source noteuspto-grants-2016_01