HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718095Generated: October 27, 2026
2-Mercaptobenzoic Acid → Methyl 2-(2-nitrophenylthio)benzoate
https://huagongshe.com/reaction/718095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Mercaptobenzoic Acid | HCID 5443 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Methyl 2-(2-nitrophenylthio)benzoate | HCID 57362693 | 76% |
Reaction Steps
A solution of 2-mercaptobenzoic acid (6.0 g, 39.0 mmol) in dimethylacetamide (20 mL) was added to a suspension of sodium hydride (60% in oil, 3.1 g, 77.5 mmol) in dimethylacetamide (15 mL). The mixture was stirred for 5 minutes and 1-fluoro-2-nitrobenzene (5.0 g, 35.5 mmol) was added. The reaction mixture was heated at 80° C. for one hour. The mixture was cooled down to room temperature and methyl iodide (7.3 mL, 117.15 mmol) was added. The reaction mixture was stirred at room temperature 16 hours. The mixture was then poor into water and extracted with a mixture of 75% ethyl acetate in hexanes (3 times). The combined organic layers were washed with water and brine, dried over sodium sulfate, filtered and evaporated. The residue was dissolved in a minimum amount of dichloromethane and hexanes was added to precipitate the product. The solid was filtered and dried to afford title compound 408 (7.81 g, 76%) as a yellow solid. MS (m/z): 312.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193749B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-9cb78712bb554d4fb72d38e3062796ac |
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| Source note | uspto-grants-2015_11 |
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