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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466059Generated: October 30, 2026

Water → 4-(5-Amino-[1,3,4]oxadiazol-2-yl)-2,6-di-tert-butyl-phenol

https://huagongshe.com/reaction/466059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyanogen BromideHCID 10476—
ReactantSodium BicarbonateHCID 516892—
Reactant3,5-Di-tert-butyl-4-hydroxybenzohydrazideHCID 10422934—
Solvent1,4-DioxaneHCID 31275—
Product4-(5-Amino-[1,3,4]oxadiazol-2-yl)-2,6-di-tert-butyl-phenolHCID 13544913062.5%

Reaction Steps

Cyanogen bromide (0.9 g, 0.0083 mole) is added to a solution of 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoic acid, hydrazide (2.2 g, 0.0083 mole) and sodium bicarbonate (0.7 g, 0.0083 mole) in dioxane (10 ml)/water (10 ml). The resulting mixture is stirred two hours at room temperature. The solution is concentrated to half volume in vacuo and the residue diluted with water. The resulting solid is filtered and recrystallized from ethyl acetate/hexane to give 1.5 g (2.4 g theor., 58%) of 4-(5-amino-1,3,4-oxadiazol-2-yl)-2,6-bis(1,1-dimethylethyl)-phenol after drying in vacuo at room temperature, mp 244°-245° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155122
Source datasetuspto-grants-1992_10
ORD IDord-c4b49e866a29467d935be610b3445b17
Source noteuspto-grants-1992_10