HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propylamine → N-[3-(4-Nitro-3-propylaminomethyl-benzenesulfinyl)-phenyl]-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N-[3-(3-Formyl-4-nitro-benzenesulfinyl)-phenyl]-benzenesulfonamide | HCID 58625065 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-[3-(4-Nitro-3-propylaminomethyl-benzenesulfinyl)-phenyl]-benzenesulfonamide | HCID 58625145 | — |
Reaction Steps
The following reaction was run under N2. A mixture of N-[3-(3-formyl-4-nitro-benzenesulfinyl)-phenyl]-benzenesulfonamide (0.0023 mol) and propylamine (0.0025 mol) in DCE (50 mL) was stirred at room temperature and NaBH(OAc)3 (0.8 g) was added. The reaction mixture was stirred overnight at room temperature, and then a NaHCO3 solution was added. The organic layer was separated, dried, and filtered, and the solvent was evaporated to yield the title compound as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383637B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-8da106186c1048bca9cbb039d1135ff4 |
| Source note | uspto-grants-2013_02 |