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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261291Generated: November 2, 2026

Water → (5-Tert-butyl-1,2-oxazol-3-yl)methanol

https://huagongshe.com/reaction/2261291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 5-t-butyl-isoxazole-5-carboxylateHCID 68779846—
SolventEthanolHCID 702—
Product(5-Tert-butyl-1,2-oxazol-3-yl)methanolHCID 10820794—

Reaction Steps

1.83 g of ethyl 5-t-butyl-isoxazole-5-carboxylate was dissolved in 18 ml of tetrahydrofuran, and 0.70 g of sodium borohydride in 10 ml of ethanol was then added. The mixture was stirred at room temperature for 10 hours. After 5 ml of water was added, the reaction mixture was concentrated to 5 ml under reduced pressure. The concentrated solution was extracted with methyl-t-butyl ether. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to obtain 0.62 g of (5-t-butyl-isoxazol-3-yl)methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846956B2
Source datasetuspto-grants-2010_12
ORD IDord-fdd8deec2e8049fd89820f13d8cb5205
Source noteuspto-grants-2010_12