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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium borohydrideHCID 4148881—
ReactantEthyl(4-methyl-2-phenyl-1,3-oxazol-5-yl)acetateHCID 14115754—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Methyl-2-phenyl-1,3-oxazol-5-yl)ethanolHCID 2194275225.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541618B2
Source datasetuspto-grants-2013_09
ORD IDord-bf8336afe9854eacabd174154118a2a4
Source noteuspto-grants-2013_09