HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 4-(4-Benzylaminosulfonylmethylbenzyl)-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Chlorosulfonylmethyl-benzyl)-nitrobenzene | HCID 21876818 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Benzylaminosulfonylmethylbenzyl)-nitrobenzene | HCID 21876751 | — |
Reaction Steps
Benzylamine (0.3 mL) was added to a solution of 4-(4-chlorosulfonylmethyl-benzyl)-nitrobenzene (100 mg) in tetrahydrofuran (4 mL). The mixture was stirred for 2 hours, poured into dilute aqueous potassium carbonate, and extracted with dichloromethane (3×15 mL). Solvents were evaporated and the residue was chromatographed on silica gel, eluting with 2% acetone in dichloromethane, to give 4-(4-benzylaminosulfonylmethylbenzyl)-nitrobenzene (44 mg) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06184242B2 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-28e5b9ba4c1a4b81aca8a9a30b41f5ac |
| Source note | uspto-grants-2001_02 |