HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307536Generated: October 25, 2026
4-Fluorobenzyl chloride → 1-[5-[(4-Fluorophenyl)methyl]-2-furanyl]ethanone
https://huagongshe.com/reaction/2307536
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | 2-Acetylfuran | HCID 14505 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[5-[(4-Fluorophenyl)methyl]-2-furanyl]ethanone | HCID 10130640 | 74% |
Reaction Steps
To 258 g (0.94 mol) of a 50% aqueous solution of zinc chloride were added 69.3 g of water, 99.0 g (0.90 mol) of 2-acetylfuran and 260 g (1.80 mol) of 4-fluorobenzylchloride. The mixture was stirred at 85° C. for 6 hours. The reaction mixture was cooled and extracted with ethylacetate. The extract was washed with 1N hydrochloric acid, washed with an aqueous sodium hydrogencarbonate solution and removed under reduced pressure. The obtained residue was distilled under reduced pressure to give 145.4 g of crude 2-acetyl-5-(4-fluorobenzyl)furan (106-121° C./0.4 mmHg). The crude product was recrystallized from isopropylalcohol/n-hexane to give 84.4 g of 2-acetyl-5-(4-fluorobenzyl)furan. Yield: 43%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06831177B1 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-bf1d1dbb5ef84e9db47ec2295b75da8f |
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| Source note | uspto-grants-2004_12 |
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