HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Phenylenediamine → N-(4-aminophenyl)butanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Phenylenediamine | HCID 7814 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-aminophenyl)butanamide | HCID 721131 | 37.6% |
Reaction Steps
To a solution of 1,4-phenylenediamine (0.5 g, 4.62 mmol) in anhydrous CH2Cl2 (15 mL) was added NMM (0.51 mL, 4.62 mmol). To the resulting mixture was added dropwise butyryl chloride (0.45 mL, 4.62 mmol) in anhydrous CH2Cl2 (5 mL) at 0° C., and stirred for 0.5 h. The reaction mixture was extracted with CH2Cl2 (20 mL) and washed with H2O (20 mL). The organic layer was dried over MgSO4 and evaporated in vacuo. The residue was purified by column chromatography over silica gel (EtOAc:hexane=1:3) to give N-(4-aminophenyl)butyramide (KYJ3-006-2, 0.31 g, 36%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166744B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-92c9587a25624274ba059df954d064ff |
| Source note | uspto-grants-2007_01 |