HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429718Generated: October 29, 2026
Sulfuryl chloride → HCID 18352666, compound
https://huagongshe.com/reaction/429718
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(2-Methylphenyl)cyclohexanone | HCID 18352669 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18352666 | HCID 18352666 | — |
Reaction Steps
Prepared in analogy with a method in Hussey, A. S. and Herr, R. R., J. Org. Chem., 24, 843 (1959). To a 500 mL round-bottomed flask equipped with nitrogen inlet was added 33.3 grams (0.177 mol) of 4-(2-methylphenyl)cyclohexanone and 200 mL methylene chloride. To the stirring solution was added drop wise over 30 minutes a solution of 17.1 mL (0.212 mol) sulfuryl chloride in 10 mL methylene chloride. The reaction was stirred 14 hours at room temperature and poured into saturated aqueous sodium bicarbonate solution. The organic layer was separated, washed again with saturated aqueous sodium bicarbonate solution, dried over sodium sulfate, and evaporated to a yellow oil, 41 grams (100%), as a mixture of diastereomers which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06319915B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-663cd621717d4d1ba6a678bcc0e88a10 |
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| Source note | uspto-grants-2001_11 |
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