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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810158Generated: November 4, 2026

Sodium methanethiolate → 5-(4-Methoxy-benzoyl)-2-methylsulfanyl-benzenesulfonamide

https://huagongshe.com/reaction/1810158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant2-Fluoro-5-(4-methoxy-benzoyl)-benzenesulfonamideHCID 44235278—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-Methoxy-benzoyl)-2-methylsulfanyl-benzenesulfonamideHCID 4423550668%

Reaction Conditions

Temperature90 °C

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, 3H). Analytics calculated for C15H15NO4S2: 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362063B2
Source datasetuspto-grants-2013_01
ORD IDord-134a9d3feece4cd0bfdef31314f5d421
Source noteuspto-grants-2013_01