HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-(4-nitrophenyl)cyclopentanecarboxylate → Ethyl [(3R)-3-(4-aminophenyl)cyclopentyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-(4-nitrophenyl)cyclopentanecarboxylate | HCID 59464325 | — |
| Reactant | Methyl 3-(4-aminophenyl)cyclopentanecarboxylate | HCID 59464327 | — |
| Reactant | Ethyl [(3R)-3-(4-aminophenyl)cyclopentylidene]acetate | HCID 86619815 | — |
| Product | Ethyl [(3R)-3-(4-aminophenyl)cyclopentyl]acetate | HCID 59464217 | — |
Reaction Steps
Following the procedure described for methyl 3-(4-aminophenyl)cyclopentanecarboxylate, replacing methyl 3-(4-nitrophenyl)cyclopentanecarboxylate (Intermediate 84(ii)) with ethyl [(3R)-3-(4-aminophenyl)cyclopentylidene]acetate, the title compound was obtained; 1H NMR δ 1.18 (t, 3H), 1.21-1.76 (m, 2H), 1.80-2.12 (m, 2H), 2.23-2.48 (m, 2H), 2.80-3.01 (m, 1H), 3.16-3.30 (m, 2H), 4.06 (q, 2H), 4.79 (s, 2H), 6.45-6.51 (m, 2H), 6.84-6.91 (m, 2H); MS m/e M+MeCN 289.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795283B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-f0cac8586b6b4eb0bd263ea61b8ab1bd |
| Source note | uspto-grants-2010_09 |