Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 22902353 | HCID 22902353 | — |
| Product | HCID 22902368 | HCID 22902368 | — |
Reaction Steps
7.3 g of 3-methoxyphenylthiobenzamide [preparation similar to Example 65B)] were dissolved in 50 ml acetone and cooled to -20° C. in a nitrogen atmosphere. A solution of 4 ml oxalyl chloride in 40 ml acetone were added slowly dropwise to this solution. Then it was stirred for 1 hour at 20° C. The crystals that settled out were drawn off and the mother liquor concentrated to approximately one-third of the original volume. A further crystal fraction was obtained. In all, 5 g of 2-(3-methoxyphenyl)-1,3-thiazole-4,5-dione were obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05679699 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-72cecb65a15f435eaa5222fb4a2a6f7b |
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| Source note | uspto-grants-1997_10 |
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