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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354355생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/354355

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물ethyl 4-[N'-(2-trifluoromethylphenyl)ureido]phenylacetateHCID 23511916—
촉매ICE protocol 1HCID 56841950—
용매TetrahydrofuranHCID 8028—
생성물[4-({[2-(Trifluoromethyl)phenyl]carbamoyl}amino)phenyl]acetic acidHCID 1725562051%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756378B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-6ba0968d7635407aae6f314deb3ed1bb
출처 메모uspto-grants-2004_06