HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636667Generated: October 31, 2026
Thiophenol → 4-Methyl-5-[(phenylthio)methyl]-1,2,3-thiadiazole
https://huagongshe.com/reaction/636667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4-Methyl-1,2,3-thiadiazol-5-yl)methanol | HCID 18411623 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Methyl-5-[(phenylthio)methyl]-1,2,3-thiadiazole | HCID 15906640 | 85% |
Reaction Steps
At an ice-cooled temperature, 3 ml of thionyl chloride was added to 0.50 g (3.8 mmol) of 4-methyl-1,2,3-thiadiazol-5-ylmethanol and stirred for 4 hours. Then, the reaction mixture was concentrated under reduced pressure, and 1.30 g (11.5 mmol) of potassium carbonate, 0.38 g (3.4 mmol) of thiophenol and 10 ml of acetone were added to the concentrate and reacted for 7 hours with heating under reflux. After the reaction was completed, the reaction mixture was cooled to room temperature, the precipitated matter was filtered off, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography using 5:1 mixture of n-hexane and ethyl acetate. Thus, 0.64 g of the objective compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06194444B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-f1c67b6cbfb941dab1e519b52726ac5c |
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| Source note | uspto-grants-2001_02 |
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