Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358751Generated: October 25, 2026

Water → 4-[3-(4-Trifluoromethanesulfonyl-phenoxy)-phenoxy]-benzoic acid

https://huagongshe.com/reaction/1358751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3-Hydroxyphenoxy)benzoic acidHCID 615389—
Reactant1-Chloro-4-(trifluoromethylsulfonyl)benzeneHCID 703324—
SolventDimethylformamideHCID 6228—
Product4-[3-(4-Trifluoromethanesulfonyl-phenoxy)-phenoxy]-benzoic acidHCID 9845963—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-(3-hydroxyphenoxy)benzoic acid (100 mg, 0.434 mmol), 4-(trifluoromethylsulfonyl)chlorobenzene (106 mg, 1 equiv.) and potassium carbonate (240 mg, 4 equiv.) in DMF was heated to 100° C. overnight. The reaction was poured into water, extracted with EtOAc, washed the organic layer with water, brine, dried and concentrated. The residue was column chromatographed to give 4-[3-(4-trifluoromethanesulfonyl-phenoxy)-phenoxy]-benzoic acid. 1HNMR (300 MHz, DMSO-d6) δ 8.09 (d, J=8.97 Hz, 2H), 7.95 (d, J=8.94 Hz, 2H), 7.56 (t, J=8.54 Hz, 1H), 7.33 (d, J=8.94 Hz, 2H), 7.10 (d, J=8.97 Hz, 2H), 7.04-7.11 (m, 3H). MS-EI m/z 438 [M+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596772B1
Source datasetuspto-grants-2003_07
ORD IDord-86a54f0463a44c3b9d31b9166ab81ecf
Source noteuspto-grants-2003_07