HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900830Generated: October 29, 2026
Sodium Chloride → HCID 23086898, compound
https://huagongshe.com/reaction/900830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2-Butyn-1-ol | HCID 12991 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 23086893 | HCID 23086893 | — |
| Reactant | HCID 23086911 | HCID 23086911 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23086898 | HCID 23086898 | — |
Reaction Steps
To 3 ml of N,N-dimethylformamide were added 300 mg of a mixture of 3-methylsulfinyl-5-phenyl-1,2,4-thiadiazole and 3-methylsulfonyl-5-phenyl-1,2,4-thiadiazole (integration ratio of 1H-NMR sulfonyl form:sulfinyl form=4:1) and 141 mg of 2-butyne-1-ol, and to the resulting mixture was added 80 mg of sodium hydride (60% oily) with ice-cooling. The mixture was stirred for 10 minutes with ice-cooling, and allowed to stand at room temperature for 18 hours. Then, the reaction mixture was poured into an aqueous saturated sodium chloride solution, and the mixture was extracted with t-butyl methyl ether. The organic layer was concentrated, and the resulting residue was subjected to silica gel column chromatography to obtain 200 mg of 5-phenyl-3-(2-butynyloxy)-1,2,4-thiadiazole (the compound (2) of the present invention).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361675B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-d03d70b8eec54ef6b83991ba83062d0e |
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| Source note | uspto-grants-2008_04 |
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