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Diethyl Ether → HCID 68659485、化合物

HRID 1945309
ノート
印刷プレビュー

反応式

HRID 1945309 の反応式
CC(C[AlH]CC(C)C)C.[Br:10][C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][C:19]=1[F:20])[N:16]([CH2:21][C:22](OCC)=[O:23])[CH:15]=[CH:14]2.[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+].CCOCC>C1COCC1>[Br:10][C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][C:19]=1[F:20])[N:16]([CH2:21][CH2:22][OH:23])[CH:15]=[CH:14]2
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 3283Diethyl EtherHCID 9357Potassium Sodium TartrateHCID 14487Diisobutylaluminum hydrideHCID 86640506ethyl (5-bromo-6-fluoro-1H-indol-1-yl)acetate

生成物 1

HCID 68659485HCID 68659485、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

DIBAL-H (1 M in hexanes) (4 mL, 4 mmol) was added to a 0° C. solution of ethyl (5-bromo-6-fluoro-1H-indol-1-yl)acetate (0.480 g, 1.60 mmol) in anhydrous THF (10 mL). The reaction was stirred at rt for 1 h, then treated with saturated aqueous Rochelle's salt and Et2O. The mixture was stirred vigorously for 30 min. The layers were separated and the aqueous layer was further extracted with Et2O. The combined organic layers were washed with brine, dried (Na2SO4), filtered, and concentrated. Chromatography over silica eluting with 60% EtOAc/hexanes afforded the desired compound as an oil.

後処理

  1. stirringThe mixture was stirred vigorously for 30 min
  2. customThe layers were separated
  3. extractionthe aqueous layer was further extracted with Et2O
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-66a680f25bcd45f598b9c183f3dfec6c
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08394969B2

反応ノート

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