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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746301Generated: October 30, 2026

Acetic Acid → 4-tert-Butylbenzoic acid

https://huagongshe.com/reaction/746301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-tert-ButyltolueneHCID 7390—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
CatalystSodium BromideHCID 253881—
Product4-tert-Butylbenzoic acidHCID 740386.4%

Reaction Steps

Analogously to Example 1, 300 g of p-tert-butyltoluene (93.3% pure) was oxidized in the presence of 50 g of acetic acid, 3 g of cobalt acetate tetrahydrate and 1.5 g of sodium bromide at 25 bar and 115°-135° C. by passing air through it to produce a gas exhaust rate of 1.5 liters per minute. The oxygen absorption ended after a reaction period of 300 minutes; then 450 g of 74.5% acetic acid was added, the dilute reaction mixture was cooled with stirring to room temperature and filtered, and the crystallizate was washed with 450g of 70% acetic acid. 311.5 g of p-tert-butylbenzoic acid resulted, in the form of white crystals of a purity of 99.6 percent by weight as determined by gas chromatography, with a terephthalic acid content of 0.16%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04603220
Source datasetuspto-grants-1986_07
ORD IDord-ce0a3f85e58a4eb1b31c67e6762ef737
Source noteuspto-grants-1986_07