Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | HCID 20491757 | HCID 20491757 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86675538 | HCID 86675538 | — |
Reaction Steps
5 mmol of ethyl 4-(bromomethyl)-2-methyl-1,3-thiazole-5-carboxylate was dissolved in 50 ml of ethanol, then 5.5 mmol of thioacetoamide was added, and the temperature was heated up to 95° C. to carry out the reaction for 4 hours. The reacted liquid was cooled down to a room temperature. Ethanol was evaporated out and then purification was carried out using column separation method with solvents of ethylacetate and hexane, obtaining ethyl 4-(mercaptomethyl)-2-methyl-1,3-thiazole-5-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08779086B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-aa8691cf92424983a6a7a54130939238 |
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| Source note | uspto-grants-2014_07 |
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