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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2352778생성일: 2026년 10월 27일

Trifluoroacetic acid → 5-(4-Nitro-benzyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2352778

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Sodium borohydrideHCID 4311764—
반응물5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-oneHCID 68700714—
생성물5-(4-Nitro-benzyl)-1,3-dihydro-indol-2-oneHCID 6870187761%

반응 단계

In a dried 250 mL round bottom flask, 20.73 mL of trifluoroacetic acid was added and then cooled to 0° C. under Ar(g). NaBH4 in pellet form (1.35 g, 35.71 mmol, ˜1.5 pellets) was added to the flask. 5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-one (as prepared in Example 7, 1.0 g, 3.55 mmol) was then added in slowly over 15 min. After the addition was completed, the reaction was allowed to warm to room temperature and was stirred for 36 hours forming a yellow foamy mixture. The mixture was poured over ice-water and allowed to warm to room temperature, during which a tan solid precipitated out of solution. The tan solid was collected by filtration and washed with water affording 5-(4-Nitro-benzyl)-1,3-dihydro-indol-2-one in 61% yield (0.589 g, 2.165 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07749530B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-5a27ecb47f3b4eb783370ed8f2280656
출처 메모uspto-grants-2010_07