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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354359Generated: October 26, 2026

Trifluoroacetic acid → 3-methyl-4-[N'-(2-trifluoromethylphenyl)ureido]phenylacetic acid

https://huagongshe.com/reaction/354359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl 3-methyl-4-[N'-(2-trifluoromethylphenyl)ureido]phenylacetateHCID 23512225—
SolventDichloromethaneHCID 6344—
Product3-methyl-4-[N'-(2-trifluoromethylphenyl)ureido]phenylacetic acidHCID 2351219977%

Reaction Steps

To a stirred solution of tert-butyl 3-methyl-4-[N′-(2-trifluoromethylphenyl)ureido]phenylacetate (1.06 g, 2.60 mmol) in CH2Cl2 (10 ml) was added TFA (10 ml) and the reaction mixture was stirred at room temperature for 4 hr. 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 3-methyl-4-[N′-(2-trifluoromethylphenyl)ureido]phenylacetic acid (702 mg, 77%) as a white crystalline powder. mp 262-263° C.; 1H-NMR (DMSO-d6) δ2.24 (s, 3 H), 3.48 (s, 2 H), 7.03 (d, J=8.3 Hz, 1 H), 7.08 (s, 1 H), 7.26-7.30 (m, 1 H), 7.61-7.69 (m, 3 H), 7.88 (d, J=8.3 Hz, 1 H), 8.39 (s, 1 H), 8.55 (s, 1 H), 12.28 (br s, 1 H); Anal. Calcd. for C17H15F3N2O3: C, 57.96; H, 4.29; N, 7.95; F, 16.18. Found: C, 57.73; H, 4.23; N, 7.92; F, 16.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756378B2
Source datasetuspto-grants-2004_06
ORD IDord-e80fc88cc5924ad1a0299469e8fa5c8c
Source noteuspto-grants-2004_06