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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484187Generated: November 1, 2026

Trifluoroacetic acid → 4-(2-(2,4-difluorophenoxy)-4-(perfluoroethyl)benzamido)benzoic Acid

https://huagongshe.com/reaction/1484187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-[[2-fluoro-4-(1,1,2,2,2-pentafluoroethyl)benzoyl]amino]benzoateHCID 90314955—
SolventDichloromethaneHCID 6344—
Product4-(2-(2,4-difluorophenoxy)-4-(perfluoroethyl)benzamido)benzoic AcidHCID 7784426322%

Reaction Conditions

Temperature40 °C

Reaction Steps

The ester obtained in the previous step was dissolved in dichloromethane (1 mL). 2,2,2-Trifluoroacetic acid (4 mL, 52.50 mmol) was added and the reaction was stirred at 40° C. for 18 hours. The excess TFA and dichloromethane was evaporated under reduced pressure. The crude product was filtered and purified by reverse phase preparative chromatography utilizing a gradient of 30-99% acetonitrile in water containing HCl as a modifier to yield 4-(2-(2,4-difluorophenoxy)-4-(perfluoroethyl)benzamido)benzoic acid (2) (31.8 mg, 22%). ESI-MS m/z calc. 487.07. found 488.5 (M+1)+; Retention time: 2.01 minutes (3 minutes run). 1H NMR (400 MHz, DMSO-d6) δ 12.80 (s, 1H), 10.92 (s, 1H), 7.98-7.87 (m, 3H), 7.87-7.75 (m, 2H), 7.68-7.59 (m, 1H), 7.57-7.45 (m, 1H), 7.44-7.31 (m, 1H), 7.22-7.13 (m, 1H), 7.11 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09421196B2
Source datasetuspto-grants-2016_08
ORD IDord-9445fbd4da374985a9d02828dfd6be76
Source noteuspto-grants-2016_08