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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364119Generated: November 4, 2026

1,2-Dimethoxyethane → Ethyl [5-benzyloxy-4'-(trifluoromethyl)biphenyl-3-yl]acetate

https://huagongshe.com/reaction/2364119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Reactant(3-Benzyloxy-5-trifluoromethanesulfonyloxy-phenyl)-acetic acid ethyl esterHCID 57755048—
SolventEthyl AcetateHCID 8857—
ProductEthyl [5-benzyloxy-4'-(trifluoromethyl)biphenyl-3-yl]acetateHCID 24771790100%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of (3-benzyloxy-5-trifluoromethanesulfonyloxy-phenyl)-acetic acid ethyl ester (108 g, 0.26 mol), 4-(trifluoromethyl)phenylboronic acid (55.6 g, 0.29 mol), 1,2-dimethoxyethane (1.1 L) and aqueous Na2CO3 (2 M, 129 mL, 0.26 mol) was mechanically stirred while purging with N2 at room temperature for 10 min. To this system was added Pd(Ph3)4 (480 mg, 0.42 mmol) and heated to reflux (95° C.) for 2.5 h. The red-brown mixture was diluted with EtOAc (0.5 L) and washed with saturated aqueous NaHCO3 solution (3×200 mL) and brine (2×200 mL). The organic fraction was dried (Na2SO4) and concentrated in vacuo. The crude mixture was purified by ISCO column chromatography to obtain (5-benzyloxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl ester (107 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08692017B2
Source datasetuspto-grants-2014_04
ORD IDord-ed5f7858c60646b6b79fc7090bea1c79
Source noteuspto-grants-2014_04