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Phenylacetone → 7-Chloro-1,2-dihydro-4-methyl-5-phenylpyrrolo[3,2,1-hi]indole

HRID 267234
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인쇄 미리보기

반응식

HRID 267234 반응식
N[N:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[CH2:4][CH2:3]1.[C:12]1([CH2:18][C:19](=O)[CH3:20])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C([O-])(=O)C.[Na+]>C(O)(=O)C>[Cl:11][C:7]1[CH:6]=[C:5]2[C:10]3=[C:9]([C:18]([C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=4)=[C:19]([CH3:20])[N:2]3[CH2:3][CH2:4]2)[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7678PhenylacetoneHCID 517045Sodium AcetateHCID 203105795-Chloro-n-aminoindoline

생성물 1

HCID 215559787-Chloro-1,2-dihydro-4-methyl-5-phenylpyrrolo[3,2,1-hi]indole

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 13 g. (0.077 mole) of 1-amino-5-chloroindoline, 10 g. (0.073 mole) of phenylacetone and 10 g. of sodium acetate in 120 ml. of glacial acetic acid was heated on a steam bath for 1 hour. The mixture was cooled, filtered and the solid material washed with acetic acid and water. The product was recrystallized from benzene-isooctane; yield 12.7 g. (65%); m.p. 202°-204°C.).

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후처리

  1. additionA mixture of 13 g
  2. temperatureThe mixture was cooled
  3. filtrationfiltered
  4. washthe solid material washed with acetic acid and water
  5. customThe product was recrystallized from benzene-isooctane

출처 및 근거

ORD 기록
ord-a84fba1b055041828ca419e557721f3d
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03941806

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