HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771864Generated: November 1, 2026
Water → Methyl 4-(4-aminophenylthio)-3-nitrobenzoate
https://huagongshe.com/reaction/1771864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Aminothiophenol | HCID 14510 | — |
| Reactant | Methyl 4-chloro-3-nitrobenzoate | HCID 735797 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | Methyl 4-(4-aminophenylthio)-3-nitrobenzoate | HCID 59376804 | 90% |
Reaction Steps
A mixture of 4-chloro-3-nitrobenzoic acid methyl ester (15.0 g, 68 mmol), 4-aminothiophenol (8.8 g, 68 mmol) and K2CO3 (11.8 g, 85 mmol) in DMF (150 mL) was heated at 90° C. for 1.5 hours, cooled to room temperature, and then poured into H2O (450 mL) under stirring. The aqueous mixture was extracted with ethyl acetate (400 mL). The extract was washed with H2O (3 times) and brine, dried over MgSO4, and evaporated to give the crude produce as orange crystal. The crude product was suspended in 150 mL of i-Pr2O and stirred at room temperature for 1 hour. The crystal was collected by filtration, washed with i-Pr2O and dried at 60° C. for 3 days under reduced pressure gave purified title compound as orange crystal (18.6 g, 90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249138B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-0d736717c6b949b4abecc32bd1afd42c |
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| Source note | uspto-grants-2016_02 |
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