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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376403생성일: 2026년 10월 24일

Dibenzofuran → (S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acid

https://huagongshe.com/ko/reaction/376403

반응식

참여 물질

역할이름HCID투입량
반응물DibenzofuranHCID 568—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물(S)-(-)-2-(Trifluoroacetamido)succinic anhydrideHCID 12197622—
용매DichloromethaneHCID 6344—
생성물(S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acidHCID 5413194448%

반응 단계

To a dichloromethane (50 mL) suspension of aluminum chloride (3.19 g, 0.024 mol) at 0° C., under an inert nitrogen atmosphere was added via a solid addition funnel an intimate mixture of N-trifluoroacetyl-L-aspartic acid anhydride (3.01 g, 0.0142 mol) and dibenzofuran (2 g, 0.0119 mol). The resulting brick-red suspension was allowed to warm to room temperature over 12 hours. The reaction mixture was poured into ice water (250 mL), and the resulting colorless biphasic mixture was extracted with ethyl acetate (4×100 mL). The combined organic extracts were washed with water (2×100 mL), brine (2×100 mL) and dried over magnesium sulfate. The mixture was filtered, and the organic solution was concentrated by evaporation of the solvent in vacuo to yield a white solid. The solid was recrystallized from 10% ethyl acetate/hexane (v/v) to give (S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acid (2.16 g, 48%) as a while solid; mp 174-176° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06020366
출처 데이터셋uspto-grants-2000_02
ORD IDord-36d7ccd7f5ce4ca6b2b4f941420f8764
출처 메모uspto-grants-2000_02