HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522773Generated: November 4, 2026
Potassium Hydroxide → HCID 89444536, compound
https://huagongshe.com/reaction/1522773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | HCID 89444584 | HCID 89444584 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 89444536 | HCID 89444536 | — |
Reaction Steps
To a solution of 1-(4-Bromo-3-methyl-phenyl)-3-(3,5-dichloro-phenyl)-4,4,4-trifluoro-3-mercapto-butan-1-one (382 mg) in a solution of potassium hydroxide (162 mg in 8 mL of water) was added a solution of Hydroxylamine-O-sulfonic acid (2 equiv.) in a solution of potassium hydroxide (243 mg in 16 mL of water). After stirring at room temperature for 30 minutes, the mixture was diluted with ethyl acetate, and washed with brine. The collected organic phases were dried over magnesium sulfate, filtered and the filtrate was evaporated under vacuo. The residue was purified by chromatography on silica gel (eluent: cyclohexane/dichloromethane) to give 3-(4-Bromo-3-methyl-phenyl)-5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isothiazole (184 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09078444B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-846150ab14334d62af8ab7bb32185e14 |
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| Source note | uspto-grants-2015_07 |
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