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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171461Generated: November 4, 2026

Pyrrolidine → 2-(3-Ethylureido)-5-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1171461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantAllyl 2-(3-ethylureido)-5-(trifluoromethyl)benzoateHCID 21075131—
SolventAcetonitrileHCID 6342—
Product2-(3-Ethylureido)-5-(trifluoromethyl)benzoic acidHCID 2226875256.5%

Reaction Steps

The allyl 2-(3-ethylureido)-5-(trifluoromethyl)benzoate (1.8 g, ca. 5.7 mmol) was dissolved in acetonitrile (50 mL) The solution was charged with pyrrolidine (1.0 mL, 12 mmol) and Ph(PPh3)4 (140 mg, 0.17 mmol) and then stirred for 2 h at RT before being concentrated in vacuo. The residue was diluted with EtOAc and this was washed successively with 1N HCl (2×) and brine (1×) before being dried (Na2SO4), filtered, and concentrated in vacuo. The residue was triturated with methylene chloride to afford pure 2-(3-ethylureido)-5-(trifluoromethyl)benzoic acid (0.89 g). 1H-NMR (300 MHz, d4-MeOH): δ 8.59 (d, 1H, J=9.6 Hz), 8.26 (d, 1H, J=1.5 Hz), 7.72 (dd, 1H, J=9.2, 1.8 Hz), 3.23 (q, 2H, J=7.3 Hz), 1.17 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-340403ba5f41454093c44107cd8e17d6
Source noteuspto-grants-2010_11