HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490730Generated: October 30, 2026
Hydrochloric Acid → HCID 58765710, compound
https://huagongshe.com/reaction/490730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 69057069 | HCID 69057069 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58765710 | HCID 58765710 | — |
Reaction Steps
2-[4-Isopropyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-propionic acid ethyl ester (1.11 g, 3.12 mmol) and tetrahydrofuran (50 mL) are cooled to 0° C. Lithium aluminum hydride (0.24 g, 6.25 mmol) is added and the resulting mixture is stirred 20 hr at room temperature. The mixture is cooled to 0° C. and 1M aqueous hydrochloric acid (50 mL) is carefully added. The mixture is then diluted with ethyl acetate (100 mL) and the layers are separated. The aqueous layer is washed with ethyl acetate (100 mL) and the organic washes are combined, washed with water and brine (50 mL each), dried over anhydrous magnesium sulfate, filtered and concentrated to constant weight to give 2-[4-Isopropyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-propan-1-ol as a pale orange oil, 1.03 g, 100%. MS (M++1) 314. The following compound is made in similar manner:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528160B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-0d4c5541198a4735972bcb24a8d3f18e |
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| Source note | uspto-grants-2009_05 |
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