Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | 3,5-Dichloro-4H-1,2,6-thiadiazin-4-one | HCID 354026 | — |
| Solvent | Trimethylamine | HCID 1146 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15593669 | HCID 15593669 | — |
Reaction Steps
In one portion 2.5 g of trimethylamine was added to a solution of 4.6 g of 3,5-dichloro-4H-1,2,6-thiadiazin-4-one in 75 ml of ethyl ether in a 250 ml flask. A solution of 2.8 g of thiophenol in 25 ml of ethyl ether was then added dropwise to the flask during a 15 minute period. The reaction was allowed to stir for 3 hrs. after which it was filtered. The filter cake was washed with ether, and the filter cake was discarded. Successively, the ether solution was washed twice with 50 ml of water and once with 50 ml of saturated sodium chloride solution. The ether solution was then dried over anhydrous sodium sulfate. The ether was evaporated, leaving a solid residue which was recrystallized from 75 ml of cyclohexane. The yellow-orange 3-chloro-5-phenylthio-4H-1,2,6-thiadiazin-4-one weighed 3.6 g, mp 99.5°-101.5° C. (Lit. mp 102.5°-103.5° C, J. Geevers and W. P. Trompen, supra.). The ir spectrum was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04100281 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-8eccee9e2971487197f948ddd7ec2406 |
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| Source note | uspto-grants-1978_07 |
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