HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647408Generated: October 30, 2026
Water → 3-Acetonylthio-2-(4-chloro-2-fluorophenyl)-2,3,4,5,6,7-hexahydro-1H-isoindol-1-one
https://huagongshe.com/reaction/647408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | 2-(4-chloro-2-fluorophenyl)-2,3,4,5,6,7-hexahydro-3-mercapto-1H-isoindol-1-one | HCID 13257592 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-Acetonylthio-2-(4-chloro-2-fluorophenyl)-2,3,4,5,6,7-hexahydro-1H-isoindol-1-one | HCID 13257594 | 73% |
Reaction Steps
In 10 ml pyridine was dissolved 1.5 g of 2-(4-chloro-2-fluorophenyl)-2,3,4,5,6,7-hexahydro-3-mercapto-1H-isoindol-1-one, and 0.6 g of chloroacetone was added dropwise to the mixture with stirring with cooling at 5° to 10° C. over a period of 10 minutes. After cooling was continued at room temperature for 2 hours, water was added to the mixture for extraction with dichloromethane. The dichloromethane layer was separated out, washed with dilute hydrochloric acid and water, successively, and dried over anhydrous sodium sulfate. The dichloromethane was distilled off under reduced pressure, and the resulting crystals were washed with a mixed solvent of ether and hexane and dried, thereby producing 1.3 g (yield of 73%) of the subject compound. Recrystallization from ethanol yielded white crystals, m.p. 131°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04409018 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-57e264504aa84c9680ad41f0026ef81d |
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| Source note | uspto-grants-1983_10 |
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