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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354393Generated: November 1, 2026

Triethylamine → 4-[(2-Methylphenyl)ureido]-2,5-difluorophenylacetic acid

https://huagongshe.com/reaction/354393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Tolyl isocyanateHCID 69194—
ReactantEthyl 2-(4-amino-2,5-difluorophenyl)acetateHCID 23512379—
SolventDimethylformamideHCID 6228—
Product4-[(2-Methylphenyl)ureido]-2,5-difluorophenylacetic acidHCID 2351190446%

Reaction Steps

To a stirred solution of ethyl 4-amino-2,5-difluorophenylacetate (323 mg, 1.5 mmol) in DMF (8 mL), were added triethylamine (0.209 ml, 1.5 mmol) and 2-methylphenyl isocyanate (0.372 ml, 3.0 mmol) at rt. The stirring was continued for 48 hour at 80° C. The reaction mixture was evaporated in vacuo, and the solid was suspended to n-hexane. The solid was collected through filtration. The solid was dissolved in THF—MeOH (1:1, v/v, 20 mL), and was added 4M NaOH (10 mL) at rt. The stirring was continued for 18 hours at rt. The reaction was poured into 1M HCl, and the resulting precipitate was collected through filtration The solid was recrystallized with CHCl3-n-hexane to give 4-[(2-methylphenyl)ureido]-2,5-difluorophenylacetic acid (214 mg, 46%) as a white solid. 1H-NMR (CDCl3) δ2.30 (s, 3H), 3.35 (m, 2H), 7.02 (m, 2H), 7.18 (d, J=7.3 Hz, 2H), 7.69 (d, J=7.8 Hz, 1H), 8.03 (m, 1H); MS (FAB) m/z 321 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756378B2
Source datasetuspto-grants-2004_06
ORD IDord-9799e6ade0c9481791206d516fdbe5b4
Source noteuspto-grants-2004_06