HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662731Generated: October 30, 2026
Chlorosulfonic acid → HCID 86625712, compound
https://huagongshe.com/reaction/1662731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | HCID 67428671 | HCID 67428671 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86625712 | HCID 86625712 | — |
| Product | HCID 86625713 | HCID 86625713 | — |
Reaction Steps
To a solution of 1.00 g of the compound obtained in Step 179-1 in CHCl3 (10 ml) was added dropwise 3.36 g of chlorosulfonic acid in CHCl3 (10 ml) over 30 minutes under ice cooling. After stirring at room temperature for one hour, the solution was poured into ice water and the resulting mixture was extracted with CHCl3. The organic layer was washed with a saturated aqueous solution of NaHCO3 and with saturated brine and then dried over MgSO4; the drying agent was separated by filtration, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography (silicagel 60N; mobile phase: EtOAc/n-hexane=1/10 to 1/5; v/v) to obtain 340 mg of 4-(methylthio)-2-(trifluoromethoxy)benzene sulfonyl chloride (179-2-a) and 212 mg of 2-(methylthio)-4-(trifluoromethoxy)benzene sulfonyl chloride (179-2-b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030499B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-cae0664ff36c4cb4a839c2ec3e233759 |
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| Source note | uspto-grants-2011_10 |
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