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HRID 354355Erstellt: 24. Oktober 2026

Hydrochloric Acid → [4-({[2-(Trifluoromethyl)phenyl]carbamoyl}amino)phenyl]acetic acid

https://huagongshe.com/de/reaction/354355

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
Eduktethyl 4-[N'-(2-trifluoromethylphenyl)ureido]phenylacetateHCID 23511916—
KatalysatorICE protocol 1HCID 56841950—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[4-({[2-(Trifluoromethyl)phenyl]carbamoyl}amino)phenyl]acetic acidHCID 1725562051%

Reaktionsschritte

To a stirred solution of ethyl 4-[N′-(2-trifluoromethylphenyl)ureido]phenylacetate (1.93 g, 5.27 mmol) in THF (10 ml) was added 1 N NaOH (10 ml) and the reaction mixture was heated under reflux for 5 hr. After cooled to room temperature, the mixture was poured into ice-1 N HCl. The resulting precipitate was collected under a reduced pressure and the crude solid was recrystallized from MeOH—CHCl3—IPE to give 4-[N′-(2-trifluoromethylphenyl)ureido]phenylacetic acid (910 mg, 51%) as a white crystalline powder. mp 224-225° C.; 1H-NMR (DMSO-d6) δ3.50 (s, 2 H), 7.18 (d, J=8.3 Hz, 2 H), 7.25-7.29 (m, 1 H), 7.40 (d, J=8.3 Hz, 2H), 7.62-7.69 (m, 2 H), 7.95-7.97 (m, 1 H), 8.06 (s, 1 H), 9.37 (s, 1 H), 12.27 (br s, 1H); Anal. Calcd. for C16H13F3N2O3: C, 56.81; H, 3.87; N, 8.28; F, 16.85. Found: C, 56.68; H, 3.87; N, 8.16; F, 16.89.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06756378B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-6ba0968d7635407aae6f314deb3ed1bb
Quellennotizuspto-grants-2004_06