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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657070Generated: November 1, 2026

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

https://huagongshe.com/reaction/1657070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyanogen BromideHCID 10476—
ReactantSodium BicarbonateHCID 516892—
Reactant3,5-Bis(1,1-dimethylethyl)-4-hydroxycinnamic acid hydrazideHCID 73097702—
Solvent1,4-DioxaneHCID 31275—
Product4-[2-(5-Amino-[1,3,4]oxadiazol-2-yl)-vinyl]-2,6-di-tert-butyl-phenolHCID 13549994752.1%

Reaction Steps

Cyanogen bromide (0.7 g, 0.0067 mole) is added to a solution of 3,5-bis(1,1-dimethylethyl)-4-hydroxycinnamic acid, hydrazide (1.9 g, 0.0067 mole) and sodium bicarbonate (0.56 g, 0.0067 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 provide 1.1 g (2.1 g theor., 52%) of (E)-4-[2-(5-amino-1,3,4-oxadiazole-2-yl)ethenyl]-2,6-bis(1,1-dimethylethyl)phenol after drying in vacuo at room temperature, mp 221° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256680
Source datasetuspto-grants-1993_10
ORD IDord-3421427410cb4241b1249b7d1943b9c7
Source noteuspto-grants-1993_10