HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254171Generated: October 31, 2026
Acetic Acid → Ethyl 3-(4-methyl-1,3-thiazol-2-yl)-3-oxopropanoate
https://huagongshe.com/reaction/254171
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Acetyl-4-methylthiazole | HCID 5324797 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 2-Methylpentane | HCID 7892 | — |
| Product | Ethyl 3-(4-methyl-1,3-thiazol-2-yl)-3-oxopropanoate | HCID 66846879 | 74% |
Reaction Steps
NaH (60% in oil, 1.34 g, 33.5 mmol) was washed with isohexane (2×14 mL), suspended in toluene (25 mL), treated with diethyl carbonate (4.7 mL, 4.6 g, 38.8 mmol), heated to 80° C., treated dropwise over 20 min with a solution of 2-acetyl-4-methylthiazole (2.72 g, 19.2 mmol) in toluene (5 mL) and stirred at 80° C. for 2 h. The mixture was cooled to 0° C., treated dropwise with HOAc (4.65 mL, 4.9 g, 81 mmol) followed by ice (25 g) and water (50 mL) and stirred for 30 min. The aqueous phase was extracted with toluene (50 mL), the combined organic phase was washed with water (50 mL), dried (MgSO4) and concentrated in vacuo to give the crude product (3 g, 74%) as a dark red oil, used in the next step without further purification; NMR δH (400 MHz, CDCl3) 1.26 (3H, t, J 7.2 Hz), 2.92 (3H, s), 4.14 (2H, s), 4.18-4.25 (2H, m) and 7.31 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875600B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-f39492cb4dc843edad1063bf49cffa23 |
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| Source note | uspto-grants-2011_01 |
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