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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160328Generated: October 26, 2026

Cesium carbonate → (+/-)-3-[4-(4-Trifluoromethyl-biphenyl-3-ylmethoxy)-phenyl]-3-(3-methylthiophen-2-yl)-propionic acid

https://huagongshe.com/reaction/1160328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-(4-Trifluoromethylphenyl)-benzyl chlorideHCID 22280138—
Reactant(+/-)-Methyl 3-(4-hydroxyphenyl)-3-(3-methylthiophen-2-yl)propanoateHCID 59132701—
SolventAcetoneHCID 180—
Product(+/-)-3-[4-(4-Trifluoromethyl-biphenyl-3-ylmethoxy)-phenyl]-3-(3-methylthiophen-2-yl)-propionic acidHCID 8661322685.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

Benzyl chloride 2.3 (113 mg, 0.434 mmol) and phenol 54.1 (100 mg, 0.362 mmol) were dissolved in acetone (1 mL) and treated with Cs2CO3 (371 mg, 1.14 mmol). The reaction was stirred at 50° C. for 16 h, filtered and concentrated. The residue was purified by column chromatography (silica gel, 30% to 60% ethyl acetate in hexanes). Eluant containing desired compound was concentrated and dissolved in a THF/MeOH/2N LiOH(aq) (1:1:1) solution (2 mL). The mixture was stirred at room temperature for 90 min., the solution was poured into 0.65 N HCl (aq.) (2 mL). The aqueous phase was extracted with dichloromethane (3×10 mL) and the combined organic phases were dried over Na2SO4. After filtration and drying, 154 mg (0.311 mmol) of carboxylic acid 54 was obtained. 1H NMR (400 MHz) (CDCl3) δ 7.43-7.70 (m, 8H), 7.21 (d, 2H, J=8.6 Hz), 7.05 (d, 1H, J=5.0 Hz), 6.92 (d, 2H, J=8.6 Hz), 6.76 (d, 1H, 5.0 Hz), 5.09 (s, 2H), 4.74 (t, 1H, J=7.8 Hz), 3.05 (d, 2H, J=7.8 Hz), 2.15 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816367B2
Source datasetuspto-grants-2010_10
ORD IDord-d40ad184df5940e1a43a37bfe88cfc4a
Source noteuspto-grants-2010_10