HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4-(4-nitrophenyl)butanoate → Methyl 4-aminobenzenebutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4-(4-nitrophenyl)butanoate | HCID 140721 | — |
| Reactant | Methyl 4-(2-nitrophenyl)butanoate | HCID 11401810 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-aminobenzenebutanoate | HCID 88628 | 41% |
Reaction Steps
A mixture of methyl 4-(4-nitrophenyl)butanoate and methyl 4-(2-nitrophenyl)butanoate (2.24 g, 10.03 mmol) and 0.2 g of 10% Pd/C in 40 mL of methanol was vigorously stirred under hydrogen air. The mixture was stirred for 4 h at room temperature (monitored by TLC), and filtered through Celite. The solvent was evaporated. The residue was purified by chromatography to give the title compound (0.80 g, 41%): NMR (400 MHz in CDCl3, Bruker AVANCE-400): δ 1.89 (m, 2H, CH2), 2.31 (t, 2H, CH2—CH2—COOMe), 2.53 (t, 2H, CH2), 3.58 (br, 2H, NH2), 3.65 (s, 3H, OMe), 6.61 (d, 2H, J=3.5 Hz, Ar—H), 6.95 (d, 2H, J=3.4 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242282B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-df227695f252421484b0bc9c38fb9c17 |
| Source note | uspto-grants-2012_08 |