HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372932Generated: October 30, 2026
Chloroform → (4aS,8aS)-3,3-Dichlorooctahydroquinolin-2(1H)-one
https://huagongshe.com/reaction/2372932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 67592240 | HCID 67592240 | — |
| Product | (4aS,8aS)-3,3-Dichlorooctahydroquinolin-2(1H)-one | HCID 71412511 | — |
Reaction Steps
28.8 g of phosphorus pentachloride were added to a solution of 23 g of cis-octahydro-1H-quinolin-2-one in 350 ml of anhydrous chloroform. To this were added dropwise 43.1 g of sulfuryl chloride in 45 ml of anhydrous chloroform at 20° to 30° C. within 30 min and the reaction mixture was stirred at the boiling point for 5 hours. After allowing to stand overnight, the mixture was neutralized with aqueous potassium carbonate cooled to 0° C. The aqueous phase was extracted twice with methylene chloride. The combined organic phases were dried over sodium sulfate and concentrated. The residue was recrystallized from ethanol with the addition of active charcoal. 32 g of pale yellow crystals, having a melting point of 176° to 177° C., were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05101039 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-16c27025e2644f15a07a938a922d8b0d |
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| Source note | uspto-grants-1992_03 |
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