HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037461Generated: October 26, 2026
1-Bromo-4-fluorobenzene → 1-(4-Fluorophenyl)but-2-en-1-one
https://huagongshe.com/reaction/2037461
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | trans-Crotonyl chloride | HCID 643131 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Fluorophenyl)but-2-en-1-one | HCID 66856453 | 10% |
Reaction Steps
To a solution of 1-bromo-4-fluorobenzene (28 g, 0.162 mol) in THF (90 mL) was added n-BuLi (70 mL, 2.5 M) at −78° C. and stirred for 1 h under nitrogen. Then to a premixed solution of CuCl (18 g, 0.16 mol) and LiCl (15 g, 0.354 mol) in THF (160 mL) at −78° C. was added the above solution quickly. The formed solution was stirred for 20 minutes, and was treated with crotonyl chloride (21 g, 0.176 mol). The resulting solution was stirred for 30 minutes. The mixture was quenched with aq NH4Cl, the organic phase was separated, concentrated to give the crude product which was purified by column chromatography to afford 1-(4-fluorophenyl)but-2-en-1-one (2.6 g, 10%). 1H NMR (400 MHz, CDCl3): δ=2.02 (d, 3H), 6.88 (m, 1H), 7.10 (m, 3H), 7.98 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575156B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-cb208c1845844655a2129863bb0be18d |
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| Source note | uspto-grants-2013_11 |
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