HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46026Generated: October 29, 2026
Hydrochloric Acid → 2-(4-Methyl-2-phenyl-1,3-oxazol-5-yl)ethanol
https://huagongshe.com/reaction/46026
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Ethyl(4-methyl-2-phenyl-1,3-oxazol-5-yl)acetate | HCID 14115754 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Methyl-2-phenyl-1,3-oxazol-5-yl)ethanol | HCID 21942752 | 25.3% |
Reaction Steps
Ethyl(4-methyl-2-phenyl-1,3-oxazol-5-yl)acetate (0.922 g, 3.76 mmol) in THF (6 mL) at rt, was added LiBH4 2M/THF (9.41 mL, 4.70 mmol). The reaction was stirred overnight at rt, then treated with 2 N HCl until pH 7. The solvent THF was removed under reduced pressure, EtOAc was added, and phases separated. The combined organic extracts were dried over MgSO4 and solvent concentrated in vacuo. The crude material was purified by Biotage using a gradient of 10 to 100% EtOAc/Hexane as solvent mixture. This gave 2-(4-methyl-2-phenyl-1,3-oxazol-5-yl)ethanol (0.193 g, 25% yield) as colorless oil. ES-MS m/z 204.2 (MH)+); HPLC RT (min.) 2.02; 1H NMR (Acetone-d6) δ 7.98-7.95 (m, 2H), 7.52-7.42 (m, 3H), 3.95 (s br, 1H), 3.82 (t, 2H)m, 2.90 (t, 2H), 2.13 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541618B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-bf8336afe9854eacabd174154118a2a4 |
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| Source note | uspto-grants-2013_09 |
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