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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261338Generated: November 2, 2026

Water → 1-(5-t-Butyl-isoxazol-3-yl)ethanol

https://huagongshe.com/reaction/2261338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-(Tert-butyl)isoxazole-3-carbaldehydeHCID 45083802—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(5-t-Butyl-isoxazol-3-yl)ethanolHCID 57736312—

Reaction Steps

1.29 g of 5-t-butyl-isoxazole-3-carbaldehyde was dissolved in 10 ml of tetrahydrofuran, and 10 ml of a 0.93 M solution of methylmagnesium bromide in tetrahydrofuran was then added. The mixture was stirred for 1 hour under ice-cooling. After water was added, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, filtered and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.18 g of 1-(5-t-butyl-isoxazol-3-yl)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846956B2
Source datasetuspto-grants-2010_12
ORD IDord-a1048bd2ad6648c3b12c89147efb694c
Source noteuspto-grants-2010_12