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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417048Generated: October 29, 2026

Cesium carbonate → 4-[3-[6-(3-Benzo[1,3]dioxol-5-yl-5-isobutyryl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester

https://huagongshe.com/reaction/417048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-[3-(6-Bromo-hexyl)-2-(ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl esterHCID 57586491—
Reactant1-(3-Benzo[1,3]dioxol-5-yl-5-hydroxy-phenyl)-2-methyl-propan-1-oneHCID 59496809—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
Product4-[3-[6-(3-Benzo[1,3]dioxol-5-yl-5-isobutyryl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl esterHCID 5949682875%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 1-(3-benzo[1,3]dioxol-5-yl-5-hydroxy-phenyl)-2-methyl-propan-1-one (109 mg) in a mixture of acetone and DMF (2:1, 3 mL) were added cesium carbonate (624 mg) and 4-[3-(6-bromo-hexyl)-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester (190 mg). The resulting mixture was stirred at 75° C. overnight. Then the insoluble material was filtered out and the filtrate was diluted with ethyl acetate and washed with water and brine. The organic extract was dried over anhydrous sodium sulfate, concentrated and purified on a silica gel column using ethyl acetate and hexanes to yield 194 mg of the title compound (75% yield). HRMS calcd for C40H50O9 [M+Na]+ 697.3347, observed 697.3344.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088936B2
Source datasetuspto-grants-2012_01
ORD IDord-f225f5aa6eb948aaab79b1b46094a556
Source noteuspto-grants-2012_01