HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751041Generated: October 28, 2026
1-Bromo-3-chloropropane → 1-(3-Chloropropyl)-3,3-difluoroindolin-2-one
https://huagongshe.com/reaction/1751041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,3-Difluoroindolin-2-one | HCID 5323821 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(3-Chloropropyl)-3,3-difluoroindolin-2-one | HCID 58046616 | 100.3% |
Reaction Steps
A solution of 3,3-difluoroindolin-2-one (836.6 mg, 4.95 mmol, 1 equiv) in N,N-dimethylformamide was cooled to 0° C. Sodium hydride (60% dispersion) (217.6 mg, 5.44 mmol, 1.1 equiv) was slowly added and the reaction was stirred as such until all bubbling had stopped. 1-bromo-3-chloropropane (1.46 ml, 14.85 mmol, 3 equiv) was added to the reaction mixture in one portion. The reaction was allowed to warm to ambient temperature and stirred as such for 16 h. The crude mixture was partitioned between ethyl acetate and water. The organic layer was dried over MgSO4, filtered, concentrated, and the residue was purified using the Biotage flash chromatography system (SNAP 50 g cartridge, Rf=0.5, gradient—5%-30% ethyl acetate in hexanes) to afford the title compound as a yellow oil (1.22 g, quant); MS for C11H10ClF2NO m/z 247.01 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156840B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-61e6303645ed4c288e2fbe0b9d36684f |
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| Source note | uspto-grants-2015_10 |
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