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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466044Generated: October 30, 2026

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

https://huagongshe.com/reaction/466044

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 diimidazole (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-hydroxybenzoic 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 HC, 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 numberUS05155122
Source datasetuspto-grants-1992_10
ORD IDord-0824ec0fa10343ca87bec1a135fffe03
Source noteuspto-grants-1992_10