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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548197Generated: October 29, 2026

Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenyl-2-butenoate → Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoate

https://huagongshe.com/reaction/548197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenyl-2-butenoateHCID 86624036—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductEthyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoateHCID 86624037100%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939552B2
Source datasetuspto-grants-2011_05
ORD IDord-58b32a7b63fa40b1b8f88a14aaa20890
Source noteuspto-grants-2011_05