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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643342Generated: October 31, 2026

5-Bromo-2-fluorobenzaldehyde → 1-(5-Bromo-2-fluorophenyl)ethanol

https://huagongshe.com/reaction/643342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-fluorobenzaldehydeHCID 736327—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product1-(5-Bromo-2-fluorophenyl)ethanolHCID 44182055—

Reaction Steps

To a solution of 5-bromo-2-fluorobenzaldehyde 101 (100 g, 0.492 mol) in ether (500 mL), cooled in an ice bath, was added a 3 M solution of methyl magnesium bromide in ether (173 mL, 0.516 mol) in a dropwise manner. The reaction mixture was stirred for 30 minutes in the ice bath. The reaction mixture was allowed to warm to room temperature and was stirred for 15 minutes. The reaction mixture was cooled in an ice bath and the reaction was quenched by addition of water in a dropwise manner. The reaction mixture was acidified with dilute hydrochloric acid. The organic layer was separated. The aqueous layer was extracted with ether for two times. The combined organic layer was dried over magnesium sulfate and evaporated under reduced pressure to afford 1-(5-Bromo-2-fluoro-phenyl)-ethanol 102 (106 g, 0.484 mol) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700601B2
Source datasetuspto-grants-2010_04
ORD IDord-2a74dde056364aa3bb67fe5efb9f2c72
Source noteuspto-grants-2010_04