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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657061Generated: November 2, 2026

Triethylamine → 5-(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3,4-oxadiazol-2(3H)-one

https://huagongshe.com/reaction/1657061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3,5-Di-tert-butyl-4-hydroxybenzohydrazideHCID 10422934—
SolventTetrahydrofuranHCID 8028—
Product5-(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3,4-oxadiazol-2(3H)-oneHCID 13550359255%

Reaction Steps

1,1'-Carbonyl dimidazole (0.8 g, 0.005 mole) is added in one portion to a stirred 0° C. solution of 3,5-bis(1,1-dimethylethyl)-4-hydrox-ybenzoic acid hydrazide (1.0 g, 0.004 mole) and triethylamine (0.6 ml, 0.004 mole) in tetrahydrofuran (12 ml). After 18 hours the mixture is concentrated in vacuo and the residue dissolved in ether. The solution is washed with aqueous 2M HCl, saturated aqueous NaHCO3, saturated aqueous NaCl, and dried over MgSO4. Filtered and concentrated in vacuo to obtain a residue which is purified by flash chromatography using 10% ethyl acetate/hexane eluent. Recrystallize from ethyl acetate/hexane to obtain 0.6 g (1.1 g theor., 55%) 5-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-1,3,4-oxadiazol-2(3H)-one, mp 246° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256680
Source datasetuspto-grants-1993_10
ORD IDord-a6efba1e3908403799d6f57f40313365
Source noteuspto-grants-1993_10