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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681572Generated: November 3, 2026

Pyridine → 4-[3-Tert.butyl-4-methoxybenzoylthio]benzoic acid

https://huagongshe.com/reaction/1681572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Mercaptobenzoic acidHCID 95738—
ReactantBenzoic acid, 3-(1,1-dimethylethyl)-4-methoxy-HCID 10488578—
SolventDichloromethaneHCID 6344—
Product4-[3-Tert.butyl-4-methoxybenzoylthio]benzoic acidHCID 1980516932%

Reaction Steps

Crude 3-(tert.butyl)-4-methoxybenzoic acid, prepared starting with 1.04 g (5 mmoles) of 3-(tert.butyl)-4-methoxybenzoic acid, described in Example 35 of French Patent No. 85 13747 (2.570.377), is dissolved in 15 ml of dichloromethane. The solution is slowly added to a mixture of 771 mg (5 mmoles) of 4-mercaptobenzoic acid and 8 ml of pyridine. The reaction mixture is stirred at ambient temperature for 8 hours, evaporated to dryness, taken up in water, acidified to pH 5 with 1N HCl and extracted with ethyl ether. The organic phase is decanted, washed with water, dried over magnesium sulfate and evaporated to dryness. The resulting residue is purified by chromatography on a silica column (eluant: ethyl ether). The solvent is evaporated and 530 mg (32% yield) of 4-[3-tert.butyl-4-methoxybenzoylthio]benzoic acid whose melting point is 220°-221° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05173289
Source datasetuspto-grants-1992_12
ORD IDord-4ca641af673646629be97e70c6a50fcf
Source noteuspto-grants-1992_12