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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525742Generated: October 27, 2026

1-Bromo-3-(trifluoromethoxy)benzene → Ethyl 4-[3-(trifluoromethoxy)phenyl]butanoate

https://huagongshe.com/reaction/1525742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-(trifluoromethoxy)benzeneHCID 519964—
ReactantHCID 178471550HCID 178471550—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-[3-(trifluoromethoxy)phenyl]butanoateHCID 8672821641%

Reaction Steps

4-Ethoxy-4-oxobutylzinc bromide solution (25 mL, 0.5 M in THF, 12.5 mmol) was added to a solution of 1-bromo-3-(trifluoromethoxy)benzene (2.6 g, 10.8 mmol) in THF (10 mL) under N2. Pd(dppf)Cl2 (1.18 g, 1.62 mmol) was added, and the reaction was heated at reflux for 3 h. The solution was concentrated and purified by silica gel chromatography (0-20% EtOAc/hexanes) to give 1.22 g (41%) of the title compound as a clear oil. 1H NMR (400 MHz, DMSO-d6): δ 1.26 (3H, t, J=7.2 Hz), 1.91-2.00 (2H, m), 2.32 (2H, t, J=7.4 Hz), 2.67 (2H, t, J=7.4 Hz), 4.13 (2H, q, J=7.2 Hz), 7.03-7.07 (2H, m), 7.11 (1H, d, J=7.7 Hz), 7.30 (1H, t, J=7.7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085534B2
Source datasetuspto-grants-2015_07
ORD IDord-26384b301ca940eaae41752b37d3fc76
Source noteuspto-grants-2015_07