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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382661Generated: November 3, 2026

Methylamine → HCID 53630783, compound

https://huagongshe.com/reaction/2382661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantC AmineHCID 6936—
ReactantThionyl ChlorideHCID 24386—
ReactantSulfuryl chlorideHCID 24648—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 53630783HCID 53630783—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2-amino-5-chloro-4-methyl-benzenesulfonic acid (3.0 g, 1.35 mmol) in dichloroethane (10 mL) is added sulfuryl chloride (4.4 mL, 3.83 mmol) and stirred at 60° C. After one hour, thionyl chloride (1.3 mL) is added and the mixture is further stirred at 100° C. for 7.0 hours. The mixture is poured into iced water and extracted with ether three times. The organic layer is washed with water and then brine, dried over sodium sulfate, and evaporated in vacuo. 1H-NMR (δ, ppm): 2.35 (s, 3H), 6.68 (s, 1H), 7.75 (s, 1H). This substituted sulfonyl chloride is reacted with a suitable amine. On reaction e.g. with methylamine, 2-amino-5-chloro-4,N-dimethylbenzenesulfonamide is formed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263590B2
Source datasetuspto-grants-2012_09
ORD IDord-45ed8bc8e6304859a6c77c6e62918eee
Source noteuspto-grants-2012_09