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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468456Generated: November 2, 2026

Sodium Hydroxide → {6-Chloro-3-methyl-4-[4-(2-trifluoromethyl-benzenesulfonylamino)-phenyl]-naphthalen-2-yl}-acetic acid

https://huagongshe.com/reaction/1468456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant{6-Chloro-3-methyl-4-[4-(2-trifluoromethyl-benzenesulfonylamino)-phenyl]-naphthalen-2-yl}-acetic acid methyl esterHCID 86695032—
SolventEthanolHCID 702—
Product{6-Chloro-3-methyl-4-[4-(2-trifluoromethyl-benzenesulfonylamino)-phenyl]-naphthalen-2-yl}-acetic acidHCID 71711647—

Reaction Steps

To a solution of {6-chloro-3-methyl-4-[4-(2-trifluoromethyl-benzenesulfonylamino)-phenyl]-naphthalen-2-yl}-acetic acid methyl ester (125 mg, 0.23 mmol) in ethanol (10 mL) was added a solution of sodium hydroxide solution (684 uL, 1.0 N) at room temperature. The resulting clear solution was stirred overnight. Then, the solvents were removed under vacuum and the residue was diluted with water (10 mL), acidified with 1.0 N hydrochloric acid and extracted with ethyl acetate (2×20 mL). The combined organic extracts were washed with brine solution (20 mL) and dried over anhydrous magnesium sulfate. Filtration of the drying agent and concentration of the solvent under vacuum provided the desired {6-chloro-3-methyl-4-[4-(2-trifluoromethyl-benzenesulfonylamino)-phenyl]-naphthalen-2-yl}-acetic acid. 1H NMR (300 MHz, DMSO-d6) δ ppm 12.47 (br. s, 1 H), 10.80 (br. s, 1 H), 8.02-8.23 (m, 1 H), 7.97-8.07 (m, 1 H), 7.85-7.95 (m, 3 H), 7.83 (s, 1 H), 7.44 (dd, J=8.8, 1.6 Hz, 1 H), 7.24 (d, J=8.5 Hz, 2 H), 7.13 (d, J=8.5 Hz, 2 H), 6.94 (d, J=1.6 Hz, 1 H), 3.81 (s, 2 H), 2.00 (s, 3 H). HRMS calcd. for C26H18ClF3NO4S [(M−H)−] 532.0602, obsd. 532.0602.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000044B2
Source datasetuspto-grants-2015_04
ORD IDord-6fcc3b2b04c6422f8c814b81313891b2
Source noteuspto-grants-2015_04