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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606283Generated: October 30, 2026

Sodium borohydride → (5-(Furan-2-yl)-1,2-oxazol-3-yl)methanol

https://huagongshe.com/reaction/606283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 5-(2-furyl)isoxazole-3-carboxylateHCID 7127810—
SolventEthanolHCID 702—
Product(5-(Furan-2-yl)-1,2-oxazol-3-yl)methanolHCID 716459188.4%

Reaction Steps

To a solution of 2.00 g of 5-furan-2-yl-isoxazole-3-carboxylic acid ethyl ester in absolute ethanol was slowly added 548 mg of sodiumborohydride at 0° C. After stirring at room temperature for 4 hrs, the reaction was quenched by addition of distilled water. The reaction solution was concentrated under reduced pressure and extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to produce 1.41 g of (5-furan-2-yl-isoxazol-3-yl)-methanol. (Yield 88%). This concentrate was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915297B2
Source datasetuspto-grants-2011_03
ORD IDord-1cea36d8160c42ebaa3d9a4b5165e8e6
Source noteuspto-grants-2011_03