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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825040Generated: November 2, 2026

3-Bromo-4-fluorobenzaldehyde → 2-Bromo-4-ethenyl-1-fluorobenzene

https://huagongshe.com/reaction/1825040

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-4-ethenyl-1-fluorobenzeneHCID 21864650—

Reaction Steps

To a suspension of Ph3PCH3Br (57 g) in THF (240 mL) at 0° C. was dropwise added n-BuLi (1.6 N, 100 mL). The resulting mixture was allowed to warm to room temperature and stirred for 1 h. After recooling to 0° C., a solution of 3-bromo-4-fluoro-benzaldehyde (20.3 g) in THF (20 mL) was added. The resulting mixture was allowed to warm to room temperature and stirred for 1 h. The reaction mixture was quenched with water, concentrated, and extracted with methylene chloride. The combined organic layer was dried over magnesium sulfate, concentrated under vacuum. The crude product was purified by flash chromatography eluting with 10% ethyl acetate in hexanes to give the title compound as an oil (18 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045551B2
Source datasetuspto-grants-2006_05
ORD IDord-67ae454a948b49f983f42cca25d7ae20
Source noteuspto-grants-2006_05