Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048485Generated: October 31, 2026

3-Methyl-1,2-oxazole-5-carbaldehyde → 1-(3-Methylisoxazol-5-yl)propan-1-ol

https://huagongshe.com/reaction/1048485

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-1,2-oxazole-5-carbaldehydeHCID 10582758—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Methylisoxazol-5-yl)propan-1-olHCID 58573217—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-methylisoxazole-5-carbaldehyde (0.801 g, 7.21 mmol) in 10 mL of THF at −78° C. was added ethylmagnesium bromide (3.60 mL, 10.81 mmol) slowly. The reaction mixture was stirred at −78° C. for 2 h, then quenched with saturated aq. NH4Cl solution, and extracted with ether (3×80 mL). The combined organic layers were dried over Na2SO4 filtered and the filtrate was evaporated to provide the crude product. The crude product was purified by chromatography on silica gel, eluting with 10 to 60% EtOAc/hexane to provide the title compound. Mass Spectrum (ESI) m/z=142.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-006e417baad3460e87c1800f85a067a3
Source noteuspto-grants-2013_10