HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-3-(4-Bromophenyl)cyclopentan-1-one → Ethyl [(3R)-3-(4-bromophenyl)cyclopentylidene]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-3-(4-Bromophenyl)cyclopentan-1-one | HCID 49833221 | — |
| Reactant | Ethyl 2-(3-(4-aminophenyl)cyclohexyl)acetate | HCID 59464273 | — |
| Reactant | Ethyl {3-[4-(benzyloxy)phenyl]cyclohexylidene}acetate | HCID 72292906 | — |
| Product | Ethyl [(3R)-3-(4-bromophenyl)cyclopentylidene]acetate | HCID 86619813 | — |
Reaction Steps
Following the general procedure described for ethyl {3-[4-(benzyloxy)phenyl]cyclohexylidene}acetate (Intermediate 89 (ii)), replacing 3-[4-(benzyloxy)phenyl]cyclohexanone with (3R)-3-(4-bromophenyl)cyclopentanone the title compound was obtained; 1H NMR δ1.18-1.23 (3H, m), 1.61-1.78 (1H, m), 2.06-2.20 (1H, m), 2.53-2.67 (3H, m), 2.84-3.04 (1H, m), 3.08-3.24 (1H, m), 4.01-4.10 (2H, m), 5.82-5.85 (1H, m), 7.24-7.28 (2H, m), 7.47-7.51 (2H, m); MS m/e MH+ 310.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795283B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-722e3fd2466149c58e30f557c9387e33 |
| Source note | uspto-grants-2010_09 |