HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenyl-2-butenoate → Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenyl-2-butenoate | HCID 86624036 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoate | HCID 86624037 | 100% |
Reaction Steps
A mixture of ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenyl-2-butenoate (40.00 g, 92.5 mmol), 5% Pd-carbon (1.00 g) and ethanol (250 mL) was stirred for 20 hours at room temperature in a hydrogen atmosphere. After filtering the catalyst, the solvent was evaporated in vacuo to give ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoate (40.18 g, 100%) as an oily product. 1H-NMR (DMSO-d6) δ: 1.04 (t, J=7.1 Hz, 3H), 2.60 (dd, J=8.0, 15.5 Hz, 1H), 2.81 (dd, J=6.8, 15.5 Hz, 1H), 3.38-3.45 (m, 1H), 3.65 (d, J=6.9 Hz, 2H), 3.94 (q, J=7.1 Hz, 2H), 4.65 and 4.66 (ABq, J=14.1 Hz, 2H), 7.20-7.24 (m, 1H), 7.28-7.32 (m, 4H), 7.90 (s, 2H), 7.99 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939552B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-58b32a7b63fa40b1b8f88a14aaa20890 |
| Source note | uspto-grants-2011_05 |