HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624221Generated: November 1, 2026
Thioacetamide → Ethyl 4-(mercaptomethyl)-2-methyl-1,3-oxazole-5-carboxylate
https://huagongshe.com/reaction/1624221
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | Ethyl 4-(bromomethyl)-2-methyl-1,3-oxazole-5-carboxylate | HCID 68242430 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-(mercaptomethyl)-2-methyl-1,3-oxazole-5-carboxylate | HCID 86675540 | 95% |
Reaction Steps
5 mmol of ethyl 4-(bromomethyl)-2-methyl-1,3-oxazole-5-carboxylate was dissolved in 50 ml of ethanol, then 5.5 mmol of thioacetoamide was added, then heated up to 90° C. to carry out the reaction for 4 hours. The reacted liquid was cooled down to a room temperature. Ethanol is evaporated out and then the product was purified using column separation with solvents of ethyl acetate and hexane, obtaining ethyl 4-(mercaptomethyl)-2-methyl-1,3-oxazole-5-carboxylate (yield 95%).
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-14b957f1312e441494120664da55986a |
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| Source note | uspto-grants-2014_07 |
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