HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659120Generated: October 27, 2026
Magnesium Carbonate → Ethyl 2-propylthiazole-5-carboxylate
https://huagongshe.com/reaction/1659120
Participants
| Role | Name | HCID | Charge |
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| Reactant | Magnesium Carbonate | HCID 11029 | — |
| Reactant | Ethyl (chloroformyl)acetate | HCID 118030 | — |
| Reactant | Butanethioamide | HCID 12454243 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 2-propylthiazole-5-carboxylate | HCID 21413783 | 79.5% |
Reaction Steps
A mixture of 38 g of thiobutyramide, 54.2 g of ethyl 2-formyl-2-chloro-acetate, 185 ml of dioxane and 22 g of magnesium carbonate was heated for 4 hours at 60°C and the precipitate formed was removed by filtration. The dioxane was distilled from the filtrate and the residue was taken up in 665 ml of a 1-1 ethyl ether-water mixture. The ether phase was recovered by decantation and was washed with aqueous 10% hydrochloric acid solution and then with water until the wash waters were neutral, dried over magnesium sulfate and distilled to dryness. The residue was distilled to obtain 57 g of ethyl 2-n-propylthiazol-5-carboxylate boiling at 95°-106°C under 0.5 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03966950 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-5de2a2621d6d43db9fa6194c20c4e9d3 |
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| Source note | uspto-grants-1976_06 |
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