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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350427Generated: November 1, 2026

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

https://huagongshe.com/reaction/350427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl 4-[N'-(2-methoxyphenyl)ureido]-3-methylphenylacetateHCID 23512525—
SolventDichloromethaneHCID 6344—
Product4-[N'-(2-methoxyphenyl)ureido]-3-methylphenylacetic acidHCID 2351226583.3%

Reaction Steps

To a stirred solution of tert-butyl 4-[N′-(2-methoxyphenyl)ureido]-3-methylphenylacetate (1.32 g, 3.56 mmol) in CH2Cl2 (15 ml) was added trifluoroacetic acid (10 ml), and the resulting mixture was heated under reflux for 30 min. The mixture was concentrated in vacuo and added water to give precipitate which was collected by filtration. The crude solid was recrystallized from EtOH/hexane to give 4-[N′-(2-methoxyphenyl)ureido]-3-methylphenylacetic acid (932 mg, 83%) as a white powder. mp 260–264° C.; 1H-NMR (CD3OD) δ 2.30 (s, 3 H), 3.55 (s, 2 H), 4.87 (s, 3 H), 6.87–6.92 (m, 2 H), 6.97–6.99 (m, 2 H), 7.10–7.24 (m, 2 H), 7.53–7.58 (m, 1 H), 8.04 (d, J=7.2 Hz, 1 H); MS (ESI) m/z 314 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-ca76329001b8450f957da3afaf20c10e
Source noteuspto-grants-2007_02