HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfinic acid → N-Pentylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfinic acid | HCID 10818 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-allyl-N-pentylphenylamine | HCID 10608235 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Pentylaniline | HCID 75865 | 93% |
Reaction Steps
p-Toluenesulfinic acid (188 ml, 1.20 mmol) was added at room temperature to a solution of N-allyl-N-pentylphenylamine(221 mg, 1.08 mmol) and tetrakis(triphenylphosphine)palladium(87.8 mg, 75.9 μmol) in dichloromethane(11 ml). The reaction mixture was stirred at room temperature for 60 minutes and saturated aqueous sodium hydrogen carbonate(6.8 ml) was added. After stirred for 5 minutes, the mixture was extracted with ether(80 ml). The extract was dried on magnesium sulfate, filterd and concentrated in vacuum. The residue was chromatographed on silica gel to give N-pentylphenylamine(164 mg) in 93% yield as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05621084 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-62cf0fb6663f4868a209d66bb418aa72 |
| Source note | uspto-grants-1997_04 |