Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468427Generated: October 31, 2026

Sodium Carbonate → {6-Fluoro-3-methyl-4-[4-(4-trifluoromethoxy-phenylsulfamoyl)-phenyl]-naphthalen-2-yl}-acetic acid methyl ester

https://huagongshe.com/reaction/1468427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Trifluoromethoxyphenyl 4-boronobenzenesulfonamideHCID 45933621—
Reactant(6-Fluoro-3-methyl-4-trifluoromethanesulfonyloxy-naphthalen-2-yl)-acetic acid methyl esterHCID 59326772—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product{6-Fluoro-3-methyl-4-[4-(4-trifluoromethoxy-phenylsulfamoyl)-phenyl]-naphthalen-2-yl}-acetic acid methyl esterHCID 8669501529%

Reaction Steps

A stirred solution of (6-fluoro-3-methyl-4-trifluoromethanesulfonyloxy-naphthalen-2-yl)-acetic acid methyl ester (0.10 g, 0.26 mmol) in dimethoxyethane (5 mL) was purged with argon for 5 minutes at room temperature. Triphenylphosphine (0.016 g, 0.06 mmol), palladium (II) acetate (0.007 g, 0.03 mmol), 4-(N-(4-(trifluoromethoxy)phenyl)sulfamoyl)phenyl-boronic acid (0.128 g, 0.35 mmol) and a 2 M aqueous solution of sodium carbonate (0.5 mL, 1.0 mmol) were added simultaneously to the reaction mixture at room temperature under argon. The reaction mixture was refluxed for 2 hours and then cooled to room temperature. Water was added and the mixture was extracted twice with ethyl acetate. The collected organic extracts were washed with water and then brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure to give the crude product, which was finally purified using flash chromatography (Biotage, 5-10% ethyl acetate-hexane) to provide {6-fluoro-3-methyl-4-[4-(4-trifluoromethoxy-phenylsulfamoyl)-phenyl]-naphthalen-2-yl}-acetic acid methyl ester (0.040 g, 29%) as a solid. MS calcd. for C27H20F4NO5S [(M−H)−] 546, obsd. 546.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000044B2
Source datasetuspto-grants-2015_04
ORD IDord-1ad6954ade61483dbf382df8464650e5
Source noteuspto-grants-2015_04