HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165074Generated: October 31, 2026
Methanesulfonyl chloride → HCID 14810655, compound
https://huagongshe.com/reaction/2165074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 14810654 | HCID 14810654 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 14810655 | HCID 14810655 | — |
Reaction Steps
To an ice-cold solution of 1-(5-trifluoromethyl-2-benzothiazolyl)ethanol (m.p. 93°-94° C., 4.94 g) in dry pyridine was added methanesulfonyl chloride (4.58 g) and the resulting solution stirred at 0° C. for 1 hour. It was poured onto water, extracted with ether and the ether layer washed with 10% hydrochloric acid (2×20 ml). The organic extract was dried, evaporated and the residue triturated with hexane to obtain the desired compound as solid, m.p. 89° C. (5.89 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04939140 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-487353019f984232aadc9f6aabc3f7c7 |
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| Source note | uspto-grants-1990_07 |
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