HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504722Generated: October 27, 2026
Acetic Acid → 2-Thiazolesulfonyl chloride
https://huagongshe.com/reaction/504722
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Sodium chloride; water | HCID 57417360 | — |
| Reactant | HCID 178527881 | HCID 178527881 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Thiazolesulfonyl chloride | HCID 11579235 | 84% |
Reaction Steps
A mixture of 1,3-thiazole-2-thiol (5.0 g), acetic acid (150 mL) and water (50 mL) was cooled to 0° C., and chlorine gas was blown into the reaction mixture at less than 20° C. When the reaction temperature ceased to rise, blowing of the chlorine gas was stopped, and nitrogen gas was blown thereinto. The reaction mixture was diluted with diethyl ether (100 mL) and saturated brine (100 mL). The organic layer was washed successively with 10% aqueous sodium sulfite solution (100 mL), aqueous sodium hydrogencarbonate (300 mL) and saturated brine (300 mL), dried over sodium sulfate, and filtrated, the filtrate was concentrated to give the title compound (6.61 g, yield 84%) as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777047B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-76b91a31d0904539b556b5c1c16ba7b2 |
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| Source note | uspto-grants-2010_08 |
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