Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexafluoropropylene | HCID 8302 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178527947 | HCID 178527947 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 73665042 | HCID 73665042 | — |
Reaction Steps
60 ml of dimethylformamide and 6.85 g of 5-(4-chlorophenyl)-2-mercapto-1,3,4-thiadiazole and 0.7 g of potassium hydroxide are stirred in an autoclave. 20 g of hexafluoropropylene are pressed in, and the reaction mixture is heated for 19 hours at 60° C. (10-12·105Pa). After cooling and release of pressure, the solution is poured into ice-water, the product is taken up in chloroform, the chloroform solution is washed with 1n sodium hydroxide solution, and the solvent is removed in vacuo, affording as reside the title compound in the form of an crystals with a melting point of 69°-70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04694014 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-60c5b464fada400eac84567af63c4503 |
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| Source note | uspto-grants-1987_09 |
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