Benzyl Alcohol → Benzyl 1-(3,4-dichlorobenzyl)-5-formyl-4-oxo-4,5,6,7-tetrahydroindole-2-carboxylate

HRID 1596536

반응식

HRID 1596536 반응식
[CH2:1]([OH:8])C1C=CC=CC=1.[H-].[Na+].[H][H].[Cl:13][C:14]1[CH:15]=[C:16]([CH:38]=[CH:39][C:40]=1[Cl:41])[CH2:17][N:18]1[C:26]2[CH2:25][CH2:24][CH2:23][C:22](=[O:27])[C:21]=2[CH:20]=[C:19]1[C:28]([O:30][CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)=[O:29].C(OCC1C=CC=CC=1)=O.Cl>C1COCC1>[Cl:13][C:14]1[CH:15]=[C:16]([CH:38]=[CH:39][C:40]=1[Cl:41])[CH2:17][N:18]1[C:26]2[CH2:25][CH2:24][CH:23]([CH:1]=[O:8])[C:22](=[O:27])[C:21]=2[CH:20]=[C:19]1[C:28]([O:30][CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)=[O:29]

참가 물질

8

실험 절차

To benzyl alcohol (1.29 g) in dry THF (20 mL) was added sodium hydride (0.48 g) and the reaction was allowed to stir until evolution of hydrogen ceased. Benzyl 1-(3,4-dichlorobenzyl)-4-oxo-4,5,6,7-tetrahydroindole-2-carboxylate (1.28 g) in THF was added, followed by benzyl formate (1.62 g), and the reaction was stirred for a further 2 hours. Upon completion, the reaction was poured into 2M HCl and extracted with ethyl acetate (2×100 mL). The organic layer was dried (MgSO4) and concentrated in vacuo. Residual benzyl alcohol was distilled from the oil under reduced pressure to afford an orange gum, which was purified by column chromatography using 20% Ethyl acetate: hexane as eluent to give the title compound as a pale white solid (1.15 g, 84%), NMR d(CDCl3) 2.60 (2H, t), 2.70 (2H, t), 5.20 (2H, s), 5.55 (2H, s), 6.75 (1H, dd), 7.10 (1H, s) 7.20-7.40 (8H, m); M/z (−) 456 (M+).

후처리

  1. extractionextracted with ethyl acetate (2×100 mL)
  2. dry with materialThe organic layer was dried (MgSO4)
  3. concentrationconcentrated in vacuo
  4. distillationResidual benzyl alcohol was distilled from the oil under reduced pressure
  5. customto afford an orange gum, which
  6. customwas purified by column chromatography

출처 및 근거

ORD 기록
ord-6bf305ab59b34135933dcb1d9e7fd940
출처 데이터셋
uspto-grants-2001_09
특허 번호
US06291507B1

연결된 노트

불러오는 중…