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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2805Generated: October 26, 2026

Ethanol → 1-(3-Furyl)-1-(4-methyl-5-oxazolyl)ethanol

https://huagongshe.com/reaction/2805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium ChlorideHCID 5234—
Reactant3-Furyl-4-methyl-5-oxazolyl ketoneHCID 54170567—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
Product1-(3-Furyl)-1-(4-methyl-5-oxazolyl)ethanolHCID 9794153—

Reaction Steps

3-Furyl-4-methyl-5-oxazolyl ketone (1 g) in dry diethylether (15 ml) at -70° C. under a nitrogen atmosphere was treated dropwise with methyllithium (1.5M solution in diethylether, 4.1 ml). After 45 minutes the reaction mixture was allowed to warm to room temperature and ethanol (2 ml) was added. The mixture was poured into saturated aqueous sodium chloride and extracted with dichloromethane. Chromatography and crystallisation then gave 1-(3-furyl)-1-(4-methyl-5-oxazolyl)ethanol identical to the material obtained in (a) above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731335
Source datasetuspto-grants-1998_03
ORD IDord-c3b3ce4ed08846c8b1f2907496e08f51
Source noteuspto-grants-1998_03