HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058355Generated: October 26, 2026
Potassium sodium tartarate → HCID 10909824, compound
https://huagongshe.com/reaction/1058355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Ethyl 4-isopropylthiazole-5-carboxylate | HCID 13015600 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10909824 | HCID 10909824 | 69% |
Reaction Steps
Diisobutylaluminum hydride (1.5M in toluene; 2.4 mL, 3.6 mmol) was added dropwise over 10 min to a solution of 4-(1-methylethyl)thiazole-5-carboxylic acid ethyl ester (Example 8; 650 mg, 3.26 mmol) in toluene (5 mL) at −75° C. After 80 min, a second portion of diisobutylaluminum hydride (1.5M in toluene; 1.1 mL, 1.65 mmol) was added dropwise over 5 min at −75° C. After 20 min the cold reaction mixture was treated with saturated aqueous potassium sodium tartrate (5 mL) and the reaction mixture was allowed to warm to room temperature over 15 min. The liquid phase was decanted from the colorless solids and the filter cake was washed with toluene. The combined organic layers were washed with 5% aqueous potassium sodium tartrate (20 mL) and brine, then dried (MgSO4), filtered and evaporated in vacuo. The resulting residue was chromatographed over silica gel (0-25% ethyl acetate/hexanes) to give 4-(1-methylethyl)thiazole-5-methanol (350 mg, 69% yield).
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-28a3aecd69d24610b5741a0cbd3a3eda |
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| Source note | uspto-grants-2003_02 |
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