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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Mercaptobenzoic acid | HCID 95738 | — |
| Reactant | Benzoic acid, 3-(1,1-dimethylethyl)-4-methoxy- | HCID 10488578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[3-Tert.butyl-4-methoxybenzoylthio]benzoic acid | HCID 19805169 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05173289 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-4ca641af673646629be97e70c6a50fcf |
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| Source note | uspto-grants-1992_12 |
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