HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510834Generated: October 31, 2026
4-Chlorobutyryl chloride → 1-(6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-yl)pyrrolidin-2-one
https://huagongshe.com/reaction/510834
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 1-(6-Amino-4-chloro-3'-fluoro-5-methylbiphenyl-2-yl)ethanone | HCID 58368430 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-yl)pyrrolidin-2-one | HCID 86666767 | 30% |
Reaction Steps
To a mixture of 1-(6-amino-4-chloro-3′-fluoro-5-methylbiphenyl-2-yl)ethanone (100 mg, 0.4 mmol) and 4-dimethylaminopyridine (52.8 mg, 0.432 mmol) in tetrahydrofuran (1 mL) was added 4-chlorobutanoyl chloride (0.044 mL, 0.40 mmol). The reaction was stirred at room temperature for 1 hour. Potassium tert-butoxide (1.0 M) in tetrahydrofuran (0.79 mL, 0.79 mmol) was added and the resulting mixture was stirred at room temperature for 2 hours, then quenched with aq. ammonium chloride and extracted with ethyl acetate. The combined organic layers were washed with water, brine, dried and evaporated. The resulting residue was purified on silica gel, eluting with 0 to 50% ethyl acetate in hexane, to give the product (40 mg, 30%). LCMS calculated for C19H18ClFNO2 (M+H)+: m/z=346.1. found: 346.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096600B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-e8fdab7e8e4d4477ab95268edd4ecead |
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| Source note | uspto-grants-2015_08 |
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