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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843999Generated: October 26, 2026

4-Hydroxy-3,5-bis(t-butyl)benzaldoxime → Benzonitrile, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-

https://huagongshe.com/reaction/843999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-3,5-bis(t-butyl)benzaldoximeHCID 328590—
ReactantSodium BicarbonateHCID 516892—
SolventDiethyl EtherHCID 3283—
SolventAcetic AnhydrideHCID 7918—
ProductBenzonitrile, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-HCID 13727454%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3,5-Di-tert-butyl-4-hydroxy-benzaldehyde oxime (3.0 grams, 8.4 mmole) in acetic anhydride (6 ml) was was refluxed for 2 hours. The mixture was cooled to 0° C. and saturated sodium hydrogencarbonate was added. The mixture was extracted with methylene chloride. The combined extracts were washed with saturated NaHCO3, dried over Na2SO4, filtered, and concentrated to give a solid. This was dissolved in diethyl ether and extracted with 1 N sodium hydroxide which was then acidified to pH 1 and extracted with ethyl acetate. The extract was dried and concentrated to a yellow solid which was recrystalized from ethyl acetate/hexane to give white crystals (1.05 g). MW 231; MS (m/e) 249 (M++NH4+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380218B1
Source datasetuspto-grants-2002_04
ORD IDord-5c09e90a1c474adaa12a8a64284234f3
Source noteuspto-grants-2002_04