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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50610Generated: October 26, 2026

Acetonitrile → 1-Naphthalenesulfonylaminoethylthioethylamine

https://huagongshe.com/reaction/50610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant1-Naphthalenesulfonyl chlorideHCID 66560—
Reactant2,2'-Thiobis(ethanamine)HCID 70096—
Product1-NaphthalenesulfonylaminoethylthioethylamineHCID 69887103—

Reaction Steps

Under ice cooling, 5.29 g of aminoethylthioethylamine was added dropwise with 120 mL of acetonitrile solution in which 1.00 g of 1-naphthalenesulfonyl chloride was dissolved, and the mixture was stirred at room temperature for two days. The reaction mixture was evaporated under reduced pressure, and then the residue was added with 500 mL of water and extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure to obtain 1.50 g of 1-naphthalenesulfonylaminoethylthioethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713473B1
Source datasetuspto-grants-2004_03
ORD IDord-85c61463f18548a999ef56fba6e12601
Source noteuspto-grants-2004_03