HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873630Generated: October 30, 2026
Sodium methanethiolate → 5-(4-Methoxy-benzoyl)-2-methylsulfanyl-benzenesulfonamide
https://huagongshe.com/reaction/873630
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 2-Fluoro-5-(4-methoxy-benzoyl)-benzenesulfonamide | HCID 44235278 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(4-Methoxy-benzoyl)-2-methylsulfanyl-benzenesulfonamide | HCID 44235506 | 68% |
Reaction Steps
To a solution of 2-fluoro-5-(4-methoxy-benzoyl)-benzenesulfonamide (0.15 g, 0.48 mmol) dissolved in dioxane (3 mL) is added sodium thiomethoxide (0.041 g, 0.57 mmol). The reaction mixture is heated at 90° C. for 4 h and then cooled to room temperature and concentrated in vacuo. The residue is partitioned between water and methylene chloride, and the aqueous phase is extracted with methylene chloride three times. The combined organic extracts are washed with a saturated sodium chloride solution, dried with magnesium sulfate, and concentrated in vacuo. Purification by silica gel chromatography (50% ethyl acetate-hexane) gives 0.11 g (68%) of the title compound as a white solid. 1H NMR (CDCl3): δ 8.4 (d, J=2 Hz, 1H), 7.90 (dd, J=8, 2 Hz, 1H), 7.80 (d, J=9 Hz, 2H), 7.50 (d, J=8 Hz, 1H), 7.00 (d, J=9 Hz, 2H), 5.20 (s, 2H), 3.90 (s, 3H), 2.65 (s, 31-1). Analytics calculated for C15H75NO4S2: C, 53.04; H, 4.48; N, 4.15. Found: C, 52.67; H, 4.57; N, 4.08. MS (m/z): 336 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975439B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-a8c934c489484bdf9ed02f734476127e |
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| Source note | uspto-grants-2015_03 |
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