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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354353Generated: November 2, 2026

Trifluoroacetic acid → 4-[N'-(2-fluorophenyl)ureido]-3-methylphenylacetic acid

https://huagongshe.com/reaction/354353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl 4-[N'-(2-fluorophenyl)ureido]-3-methylphenylacetateHCID 23512195—
SolventDichloromethaneHCID 6344—
Product4-[N'-(2-fluorophenyl)ureido]-3-methylphenylacetic acidHCID 2351211279%

Reaction Steps

To a stirred solution of tert-butyl 4-[N′-(2-fluorophenyl)ureido]-3-methylphenylacetate (1.25 g, 3.49 mmol) in CH2Cl2 (10 ml) was added TFA (10 ml) and the reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated to a small volume and poured into ice-H2O. The resulting precipitate was collected under a reduced pressure and the crude solid was recrystallized from MeOH—CHCl3—IPE to give 4-[N′-(2-fluorophenyl)ureido]-3-methylphenylacetic acid (830 mg, 79%) as white needles. 1H-NMR (DMSO-d6) δ2.23 (s, 3 H), 3.47 (s, 2 H), 6.96-7.30 (m, 5 H), 7.74-7.76 (m, 1 H), 8.17-8.20 (m, 1 H), 8.33 (s, 1 H), 8.94 (s, 1 H), 12.27 (br s, 1 H); Anal. Calcd. for C16H15FN2O3: C, 63.57; H, 5.00; N, 9.27; F, 6.28. Found: C, 63.28; H, 5.00; N, 9.14; F, 6.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756378B2
Source datasetuspto-grants-2004_06
ORD IDord-909e7d23911b423698c9166cfe52b094
Source noteuspto-grants-2004_06