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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723068Generated: November 2, 2026

1,4-Dibromobenzene → HCID 14518743, compound

https://huagongshe.com/reaction/1723068

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-4'-fluoroacetophenoneHCID 120248—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14518743HCID 1451874345%

Reaction Steps

Part A. A solution of 1,4-dibromobenzene (20.0 g, 0.08 mole) in tetrahydrofuran (200 mL) was cooled to -70+ and treated dropwise with n-butyllithium (1.6 M in hexane; 50 mL, 0.08 mole). The solution was stirred at this temperature for 60 minutes, then was treated dropwise with 4-fluorophenacyl chloride (13.8 g, 0.08 mole). The reaction was stirred at -70° overnight, then warmed to 0° for 3 hours. Saturated aqueous ammonium chloride was added, and the aqueous phase was separated. The aqueous phase was extracted with dichloromethane, and the combined organic phases were washed with saturated brine, then dried (Na2SO4) and concentrated under reduced pressure. The crude product was chromatographed on silica gel with 9:1 hexane/ethyl acetate to provide 2-(4-fluorophenyl)-2-(4-bromophenyl)-oxirane as an oil (10.5 g, 45% yield). NMR (CDCl3) 7.5-6.9(8H), 3.3-3.1(2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859693
Source datasetuspto-grants-1989_08
ORD IDord-5402cfc0e5ba4907bf54f14d126e4a14
Source noteuspto-grants-1989_08