HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559693Generated: October 29, 2026
Propanal → 2-Thiazolemethanol, -alpha--ethyl-
https://huagongshe.com/reaction/559693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propanal | HCID 527 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Thiazolemethanol, -alpha--ethyl- | HCID 15785702 | — |
Reaction Steps
A 1.3 M solution of i-PrMgCl.LiCl (2.65 mL, 3.44 mmol) under an atmosphere of argon was cooled to −15° C. and treated with a solution of 2-bromothiazole (0.56 g, 3.4 mmol) in anhydrous THF (1 mL). The reaction mixture was then allowed to warm to 0° C. over 15 minutes. Propionaldehyde (0.25 mL, 3.4 mmol) was added and the solution was allowed to warm to room temperature over 18 hours. The solution was poured into saturated aqueous ammonium chloride (50 mL) containing crushed ice. The aqueous layer was extracted with EtOAc (50 mL) and washed with saturated aqueous sodium bicarbonate (100 mL). The aqueous layer was again extracted with EtOAc (50 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The material was purified by silica gel chromatography eluting with a gradient of 0-10% methanol in dichloromethane to afford 1-thiazol-2-yl-propan-1-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063065B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-0642320d8446462b95f4acc89f7bc0bc |
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| Source note | uspto-grants-2011_11 |
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