HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944490Generated: October 29, 2026
Toluene → (3,4-Dichloroisothiazol-5-yl)methanol
https://huagongshe.com/reaction/1944490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,4-Dichloro-5-isothiazolecarboxylic acid | HCID 49837 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (3,4-Dichloroisothiazol-5-yl)methanol | HCID 16723166 | 59.2% |
Reaction Steps
A mixture of 3,4-dichloroisothiazole-5-carboxylic acid (2.0 g) and toluene (20 mL) was treated with thionyl chloride (5.0 mL) and N,N-dimethylformamide (0.5 mL), and the resulting mixture was heated at 100° C. for 16 hours. The mixture was concentrated under reduced pressure and the residue was dissolved in tetrahydrofuran (5.0 mL). The mixture was cooled to −78° C. and treated dropwise over a period of 1 hour with a 2.0 M solution of sodium borohydride in N,N-dimethylformamide (8.5 mL). The mixture was stirred at −78° C. for 5 minutes, diluted with 1.0 M aqueous hydrochloric acid solution and extracted with ethyl acetate. The combined organic extract was washed with saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with a mixture of cyclohexane and dichloromethane (1:0 to 0:1 by volume) to afford the title compound as a pale yellow solid (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394836B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-e0db55158c1c439b802d8b5b3a1f3c86 |
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| Source note | uspto-grants-2013_03 |
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