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Acetone → 5-Fluoro-3-isopropylidene-1,3-dihydro-indol-2-one

HRID 1805357
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인쇄 미리보기

반응식

HRID 1805357 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[CH2:5]2.[CH3:12][C:13]([CH3:15])=O.N1CCCCC1>CO>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=[C:13]([CH3:15])[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 180AcetoneHCID 8082PiperidineHCID 37310125-fluoro-1,3-dihydro-2H-indol-2-one

생성물 1

HCID 672305505-Fluoro-3-isopropylidene-1,3-dihydro-indol-2-one수율 68%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 5-fluoro-1,3-dihydro-indol-2-one (2.84 g, 20 mmol), acetone (2.2 mL, 30 mmol) and piperidine (0.8 mL, 8 mmol) in methanol (100 mL) was heated to reflux for 16 hours. Then the reaction mixture was allowed to cool to room temperature. The solid was collected by filtration, washed with methanol (20 mL) and dried in vacuo to afford 5-fluoro-3-isopropylidene-1,3-dihydro-indol-2-one (2.6 g, 68%) as powder.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 16 hours
  3. filtrationThe solid was collected by filtration
  4. washwashed with methanol (20 mL)
  5. customdried in vacuo

출처 및 근거

ORD 기록
ord-812991ae89c84fd390eb3e99cbf27e4b
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354443B2

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