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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454035Generated: October 30, 2026

Hydrochloric Acid → 2-(4-Methyl-2-phenyl-1,3-oxazol-5-yl)ethanol

https://huagongshe.com/reaction/1454035

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 2N HCl until pH 7. The solvent THF was removed under reduced pressure, EtOAc was added, and phases separated. The combined organics 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. 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 numberUS07476742B2
Source datasetuspto-grants-2009_01
ORD IDord-8a342a2fc8e244eebea77084ae3bffdb
Source noteuspto-grants-2009_01