HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373116Generated: October 31, 2026
2-Mercaptobenzoic Acid → 2-[(3-Methoxyphenyl)sulfanyl]benzoic acid
https://huagongshe.com/reaction/2373116
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Mercaptobenzoic Acid | HCID 5443 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 1-iodo-3-methoxy- | HCID 69839 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-[(3-Methoxyphenyl)sulfanyl]benzoic acid | HCID 13154000 | — |
Reaction Steps
First, 2-(3-methoxyphenylthio)benzoic acid was prepared. A stirred mixture of thiosalicylic acid (3.57 g, 23 mmol), 3-iodoanisole (5.42 g, 23 mmol), potassium carbonate (7.04 g, 51 mmol), copper powder (0.29 g, 5 mmol), and N-methylpyrrolidinone (75 mL) was deaerated by sparging with nitrogen for 10 min, heated at 165° C. for 2 h, and then cooled to ambient. The reaction mixture was poured onto a mixture of 500 g of ice plus 40 mL of concentrated HCl. The resulting precipitate was collected, washed with water, and dried. The precipitate was dissolved in acetone and filtered through Celite, then concentrated to deposit a crude product. The product was purified by recrystallization from aqueous ethanol. A tan powder was obtained, mass: 4.60 g (76% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459263B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-0536f15731294b0d91a9b24a06ada3c7 |
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| Source note | uspto-grants-2008_12 |
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