HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058353Generated: October 26, 2026
Ethyl Acetate → (Dimethyl-1,3-thiazol-5-yl)methanol
https://huagongshe.com/reaction/1058353
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl 2,4-dimethylthiazole-5-carboxylate | HCID 603810 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (Dimethyl-1,3-thiazol-5-yl)methanol | HCID 2776250 | 91% |
Reaction Steps
To a suspension of lithium aluminum hydride (563 mg, 14.8 mmol) in diethyl ether (25 mL) at 0° C. was added ethyl-2,4-dimethylthiazole-5-carboxylate (2.5 g, 13.5 mmol) in three portions. The reaction mixture was allowed to stir at 0° C. for 10 min, then at room temperature for 24 h. Ethyl acetate (65 mL) was added very slowly dropwise at 0° C. The reaction mixture was then added slowly to an aqueous solution of potassium sodium tartrate (30% w/v; 20 mL) and stirred for 2 h. The layers were separated and the aqueous layer was re-extracted with ethyl acetate (1×30 mL). The combined organic layers were dried (MgSO4), filtered, evaporated under reduced pressure. The resulting colorless solid was dried under high vacuum to give 2,4-dimethylthiazole-5-methanol (1.7 g, 91% yield). This material was used in a subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515124B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-d85fac8774ac422582c6725eb42a1bd3 |
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| Source note | uspto-grants-2003_02 |
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