HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905186Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 12917757, compound
https://huagongshe.com/reaction/905186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 4,5,6,7-Tetrahydro-4-benzothiazolemethanol | HCID 12917751 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 12917757 | HCID 12917757 | 72% |
Reaction Steps
9.95 g (52 mmoles) p-toluenesulfonyl chloride are added portionwise to a mixture of 8 g (47 mmoles) of the above derivative (IV) and 15 g anhydrous pyridine, while maintaining the temperature at 10° C. After stirring for 24 hrs at room temperature, the mixture is hydrolyzed and is then extracted with ethyl acetate. The combined organic phases are washed with water, dried and evaporated. The residual oil crystallizes slowly. The product is recristallyzed from boiling isopropyl oxide, on cooling. Yield: 72%. M.p.=64°-65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04423056 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-3a78217760a7447393faf6380ab336fb |
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| Source note | uspto-grants-1983_12 |
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