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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468311Generated: November 3, 2026

Methyl iodide → HCID 86658458, compound

https://huagongshe.com/reaction/1468311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86658459HCID 86658459—
SolventDimethylformamideHCID 6228—
ProductHCID 86658458HCID 86658458—

Reaction Conditions

Temperature40 °C

Reaction Steps

Potassium carbonate (177 mg, 1.28 mmol), DMF (2 ml) and MeI (60 μl) were added to the compound (230 mg, 0.65 mmol) obtained in Step 1, followed by stirring at 40° C. for 6 hours. Potassium carbonate (44.3 mg) and MeI (40 μL) were supplemented and the mixture was stirred overnight. After the solvent was removed by distillation, the mixture was purified according to the purification step A to give the crude product of 3-{methyl[(2-nitrophenyl)sulfonyl]amino}benzenesulfonic acid (160 mg). This crude product (144 mg, 0.39 m ml) was dissolved in DMF (3 ml), and cesium carbonate (126 mg, 0.39 mmol) and thiophenol (40 μl, 0.39 mmol) were added to the solution. The mixture was stirred at 50° C. overnight. After the solvent was removed by distillation, the mixture was purified in accordance with the purification step A to give the crude product of 3-(methylamino)benzenesulfonic acid (84.1 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000208B2
Source datasetuspto-grants-2015_04
ORD IDord-3de7552e4c5645079709097b3290ad53
Source noteuspto-grants-2015_04