HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 1-Naphthalenesulfonylaminoethylthioethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-Naphthalenesulfonyl chloride | HCID 66560 | — |
| Reactant | 2,2'-Thiobis(ethanamine) | HCID 70096 | — |
| Product | 1-Naphthalenesulfonylaminoethylthioethylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713473B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-85c61463f18548a999ef56fba6e12601 |
| Source note | uspto-grants-2004_03 |