Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900534Generated: October 30, 2026

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

https://huagongshe.com/reaction/900534

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 numberUS07358386B2
Source datasetuspto-grants-2008_04
ORD IDord-eb33e1ca2440475399e49c225c8199e8
Source noteuspto-grants-2008_04