HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Anilinophenyl 4-(4-nitrophenyl)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-(4-Nitrophenyl)butyric acid | HCID 24047 | — |
| Reactant | 4-Hydroxydiphenylamine | HCID 31208 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Anilinophenyl 4-(4-nitrophenyl)butanoate | HCID 22646437 | 89% |
Reaction Steps
0.98 g (6.02 mmol) of 1,1′-carbonyldiimidazole is slowly added at 20° C. to a solution of 1.25 g (5.96 mmol) of 4-nitrophenylbutyric acid in 25 ml CH2Cl2. The reaction mixture is agitated for 30 minutes before the addition of 1 g (5.42 mmol) of 4-hydroxydiphenylamine. After agitation for 3 hours, the reaction is stopped by the addition of 3 ml of MeOH and the solvent is evaporated under vacuum. The evaporation residue is purified on a silica column (eluent: Heptane/AcOEt: 100/0 to 80/20). A yellow solid is obtained with a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809090B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-5469ec2036f44108a9d2609512fabd9f |
| Source note | uspto-grants-2004_10 |