HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723068Generated: November 2, 2026
1,4-Dibromobenzene → HCID 14518743, compound
https://huagongshe.com/reaction/1723068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Chloro-4'-fluoroacetophenone | HCID 120248 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14518743 | HCID 14518743 | 45% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04859693 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-5402cfc0e5ba4907bf54f14d126e4a14 |
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| Source note | uspto-grants-1989_08 |
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