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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216454Generated: November 3, 2026

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

https://huagongshe.com/reaction/2216454

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 numberUS07112597B2
Source datasetuspto-grants-2006_09
ORD IDord-00b1384ff35e49a9bff57a819777468e
Source noteuspto-grants-2006_09