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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960160Generated: October 30, 2026

Oxygen → 4-tert-Butylbenzaldehyde

https://huagongshe.com/reaction/1960160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
Reactant4-tert-ButyltolueneHCID 7390—
Reactant4-tert-Butylbenzoic acidHCID 7403—
Reactant1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trioneHCID 10419723—
SolventAcetic AcidHCID 176—
Product4-tert-ButylbenzaldehydeHCID 70324—

Reaction Steps

In 3 mL of acetic acid was dissolved 315 mg of p-t-butyltoluene to give a solution, and the solution was combined with 156 mg of the catalyst C and 42 mg of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (hereinafter also referred to as “THICA”), followed by stirring at 100° C. in an oxygen atmosphere for 6 hours. The reaction mixture was analyzed through gas chromatography to find that p-t-butylbenzoic acid and p-t-butylbenzaldehyde were produced in yields of 84.5% and 1.4%, respectively, with a conversion from p-t-butyltoluene of 99.7%. The catalyst C was separated from the reaction mixture through filtration, washed with ethyl acetate two times, dried at room temperature (25° C.) under reduced pressure, and thereby recovered as a catalyst C1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410308B2
Source datasetuspto-grants-2013_04
ORD IDord-48c3cc297a274581904be5fd07951a7d
Source noteuspto-grants-2013_04