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1-[4-(Hydroxymethyl)phenyl]-2-cyanoindole → 1-(4-Formylphenyl)-2-cyanoindole

HRID 1769202
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반응식

HRID 1769202 반응식
[C:1]([C:3]1[N:4]([C:12]2[CH:17]=[CH:16][C:15]([CH2:18][OH:19])=[CH:14][CH:13]=2)[C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2)#[N:2]>O1CCCC1.[O-2].[O-2].[Mn+4]>[CH:18]([C:15]1[CH:16]=[CH:17][C:12]([N:4]2[C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH:11]=[C:3]2[C:1]#[N:2])=[CH:13][CH:14]=1)=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 103546391-[4-(Hydroxymethyl)phenyl]-2-cyanoindole

생성물 1

HCID 189468581-(4-Formylphenyl)-2-cyanoindole수율 68.4%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 8028Tetrahydrofuran용매

실험 절차

1.0 g (0.0038 mole) of 2-cyano-1-[4-(hydroxymethyl)phenyl]indole was dissolved in 150 ml tetrahydrofuran, 10.0 g of activated manganese dioxide was added, and the mixture stirred at room temperature for 16 hours. The reaction was filtered and the filtrate evaporated to an oil, which was crystallized from a mixture of methyl-t-butyl ether and hexane 1:1 to give 0.63 g (0.0026 mole) of 1-(4-formylphenyl)-2-cyanoindole as an oil.

후처리

  1. filtrationThe reaction was filtered
  2. customthe filtrate evaporated to an oil, which
  3. customwas crystallized from a mixture of methyl-t-butyl ether and hexane 1:1

출처 및 근거

ORD 기록
ord-ee3e1bbf0a8541ada69614329165e091
출처 데이터셋
uspto-grants-1995_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05380739

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