HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378837Generated: October 31, 2026
Carbon Dioxide → Methyl 4-methylthiazole-2-carboxylate
https://huagongshe.com/reaction/378837
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 4-Methylthiazole | HCID 12748 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Methyl 4-methylthiazole-2-carboxylate | HCID 11435075 | — |
Reaction Steps
To a solution of 4-methylthiazole (10 g) in anhydrous tetrahydrofuran (200 ml) was added n-butyl lithium in hexane (34.65 ml of 1.6M solution) dropwise at −78° C. The solution was stirred at −78° C. for 1 hour, at which point carbon dioxide gas was passed through the solution for 20 mins at −78° C. The solution was then allowed to warm to room temperature over 2 hours, the precipitate was filtered off, dissolved in methanol (200 ml) and added to methanolic hydrogen chloride (200 ml). The solution was stirred at room temperature overnight. The solvent was removed under vacuum and diethyl ether was added to the residue. The resultant solid was filtered off to yield the title compound as a white solid (2.2 g). 1H NMR (250 MHz, DMSO) δ 2.44 (3H, s), 3.89 (3H, s), 7.74 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06297235B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-9f836ff1f4da4214ae2d6060d0754106 |
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| Source note | uspto-grants-2001_10 |
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