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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54419Generated: November 1, 2026

Hydrogen Peroxide → [5-(Methoxymethyl)-1,2-oxazol-3-yl]methanol

https://huagongshe.com/reaction/54419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantLithium tri-s-butylborohydrideHCID 3611392—
Reactant3-Carbonylethoxy-5-methoxymethyl-isoxazoleHCID 19958788—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[5-(Methoxymethyl)-1,2-oxazol-3-yl]methanolHCID 19958730—

Reaction Steps

To a solution of 6.55 g of 3-carbonylethoxy-5-methoxymethyl-isoxazole in 70 ml dry tetrahydrofuran were added 77.6 ml of a 1 N solution of L-selectride® at 0° C. The solution was stirred overnight at room temperature. After cooling to 0° C. 13 ml of water and 33 ml of ethanol were added, then simultaneously 33 ml of a 6 N solution of sodium hydroxide and 49 ml hydrogen peroxide were added with caution. After stirring for half an hour the supernatant was decanted, the residue washed several times with methylene chloride. The aqueous phase was extracted with dichloromethane in an extraction apparatus for one day. The organic phase was dried over sodium sulfate and the solvent evaporated to give 4.1 g product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622953
Source datasetuspto-grants-1997_04
ORD IDord-786793f924a748b88eb7d99d760a55c7
Source noteuspto-grants-1997_04