Sodium hydride → HCID 54376915、化合物

HRID 963102ノート

反応式

HRID 963102 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([O:12][CH2:13][CH3:14])=[O:11].[H-].[Na+].Br[CH2:18][C:19]([O:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:20]>CN(C)C=O>[CH2:13]([O:12][C:10]([C:2]1[N:1]([CH2:18][C:19]([O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[O:20])[C:9]2[C:4]([CH:3]=1)=[CH:5][CH:6]=[CH:7][CH:8]=2)=[O:11])[CH3:14]

参加物

5

実験手順

Ethyl indole-2-carboxylate (22 g) was dissolved in dimethylformamide (150 ml), and sodium hydride (including 60% oil, 5.12 g) was gradually added with stirring. Then, benzyl bromoacetate (19.2 ml) was added, and the mixture was stirred for 3 hours. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was concentrated under reduced pressure. The residue thus obtained as a solid was subjected to silica gel column chromatography and eluted with a mixed solvent of ethyl acetate and hexane to give benzyl 2-ethoxycarbonyl-indole-1-acetate (28.9 g) as an oil. This compound (32.5 g) was dissolved in ethanol (350 ml), and hydrogenated in the presence of palladium/carbon (10%) catalyst at 1 atm. The catalyst was filtered off, and the solvent was concentrated under reduced pressure. The obtained residue was crystallized from isopropyl ether to give 10.22 g of 2-ethoxycarbonyl-indole-1-acetic acid.

後処理

  1. stirringthe mixture was stirred for 3 hours
  2. customThe reaction mixture was partitioned between ethyl acetate and water
  3. washThe organic layer was washed with saturated brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationThe solvent was concentrated under reduced pressure
  6. customThe residue thus obtained as a solid
  7. washeluted with a mixed solvent of ethyl acetate and hexane

出典と根拠

ORDレコード
ord-d3b147ad810b4f0e89b85b2f8e841ee5
出典データセット
uspto-grants-1998_06
特許番号
US05760032

反応ノート

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