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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54540Generated: October 28, 2026

Water → 5-(4-Cyanophenyl)-3-hydroxymethyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/54540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Ethoxycarbonyl-5-(4-cyanophenyl)-1,2,4-oxadiazoleHCID 19959148—
SolventMethanolHCID 887—
Product5-(4-Cyanophenyl)-3-hydroxymethyl-1,2,4-oxadiazoleHCID 1995916996.7%

Reaction Steps

To a solution of 5-(4-cyanophenyl)-3-ethoxycarbonyl-1,2,4-oxadiazole (5.0 g) in methanol (50 ml)--tetrahydrofuran (50 ml) was added sodium borohydride (0.93 g) at 0° C. After stirring at 5°-10° C. for 1 hour, the mixture was poured into water and extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was recrystallized from diethyl ether to give 5-(4-cyanophenyl)-3-hydroxymethyl-1,2,4-oxadiazole (4.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622976
Source datasetuspto-grants-1997_04
ORD IDord-008dbd1864a042c18c6448049da19547
Source noteuspto-grants-1997_04