Phosphonium, hexyltriphenyl-, bromide (1:1) → 5-Chloro-2-hept-1-enyl-1H-indole

HRID 2406673

반응식

HRID 2406673 반응식
[Br-].[CH2:2]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[Li+].C[Si]([N-][Si](C)(C)C)(C)C.[Cl:37][C:38]1[CH:39]=[C:40]2[C:44](=[CH:45][CH:46]=1)[NH:43][C:42]([CH:47]=O)=[CH:41]2>C1COCC1>[Cl:37][C:38]1[CH:39]=[C:40]2[C:44](=[CH:45][CH:46]=1)[NH:43][C:42]([CH:47]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7])=[CH:41]2

참가 물질

5

반응물 3

HCID 2724569Phosphonium, hexyltriphenyl-, bromide (1:1)HCID 2733832Lithium HexamethyldisilazideHCID 122033185-Chloro-1H-indole-2-carbaldehyde

생성물 1

HCID 687488825-Chloro-2-hept-1-enyl-1H-indole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To the cold suspension of hexyl-triphenyl-phosphonium bromide in THF was added LiHMDS in THF and the mixture was stirred for 30 minutes and then the solution of 5-chloro-1H-indole-2-carbaldehyde was added to the reaction mixture and stirred for 3 hours. The reaction was quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The product, 5-chloro-2-hept-1-enyl-1H-indole was purified by column chromatography.

후처리

  1. stirringstirred for 3 hours
  2. customThe reaction was quenched with saturated ammonium chloride solution
  3. extractionextracted with ethyl acetate
  4. customThe product, 5-chloro-2-hept-1-enyl-1H-indole was purified by column chromatography

출처 및 근거

ORD 기록
ord-6ba67f2cc1b5452ca7cc6b6309b94b4b
출처 데이터셋
uspto-grants-2014_08
특허 번호
US08809382B2

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