HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750797Generated: October 30, 2026
Potassium Carbonate → 2-Chloro-1-fluoro-4-(3,3,3-trifluoroprop-1-en-2-yl)benzene
https://huagongshe.com/reaction/1750797
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Propene, 2-bromo-3,3,3-trifluoro- | HCID 272696 | — |
| Reactant | 3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride) | HCID 2734660 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-1-fluoro-4-(3,3,3-trifluoroprop-1-en-2-yl)benzene | HCID 66823885 | 62.3% |
Reaction Steps
A mixture of (3-chloro-4-fluorophenyl)boronic acid (300 mg, 1.72 mmol), 2-bromo-3,3,3-trifluoroprop-1-ene (331 mg, 1.89 mmol), K2CO3 (474 mg, 3.44 mmol) and Pd(PPh3)2Cl2 (25 mg, 0.035 mmol) in THF (2 mL) and H2O (1 mL) was heated at 80° C. in a sealed tube for 3 h. The mixture was cooled to rt and partitioned between EA (20 mL) and H2O (20 mL). The aqueous layer was extracted with EA (20 mL) and the combined organic layers were dried over Na2SO4. The solvent was removed under reduced pressure and the crude product was purified by column chromatography on silica gel elute with PE to give 2-chloro-1-fluoro-4-(3,3,3-trifluoroprop-1-en-2-yl)benzene (240 mg, 62.3% yield) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156860B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-1fee94b06d9746658b63511037276c13 |
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| Source note | uspto-grants-2015_10 |
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