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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466735Generated: October 30, 2026

3-Bromo-4-fluorobenzaldehyde → 2-Fluoro-5-formylbenzonitrile

https://huagongshe.com/reaction/1466735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
ReactantHCID 178418546HCID 178418546—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Fluoro-5-formylbenzonitrileHCID 2769582107.3%

Reaction Steps

To NMP (40 ml) were added 3-bromo-4-fluorobenzaldehyde (10 g, 0.05 mol) and CuCN (5 g, 0.055 mol). The resulting mixture was heated at 170 for 24 h until the reaction finished (monitored by TLC), and cooled to 80, 10 g of celite was added and stirred for 1 h at this temperature. The reaction mixture then was cooled to room temperature, and partitioned between ethyl acetate (250 ml) and water (125 ml), the organic phase was washed with water and brine, dried, filtered, and concentrated to give the crude. Then the crude was purified by column chromatography on silica gel (Petroleum ether:Ethyl Acetate=4:1) to afford target compound (8 g, 100%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999985B2
Source datasetuspto-grants-2015_04
ORD IDord-919069b4e75b45b1b091e2370b116aed
Source noteuspto-grants-2015_04