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Enantholactam → 1-Pent-4-enyl-azocan-2-one

HRID 10179
ノート
印刷プレビュー

反応式

HRID 10179 の反応式
[H-].[Na+].[NH:3]1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][C:4]1=[O:11].Br[CH2:13][CH2:14][CH2:15][CH:16]=[CH2:17]>CN(C)C=O>[CH2:17]([N:3]1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][C:4]1=[O:11])[CH2:16][CH2:15][CH:14]=[CH2:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 12657EnantholactamHCID 24758Sodium hydrideHCID 707041-Pentene, 5-bromo-

生成物 1

HCID 219785471-Pent-4-enyl-azocan-2-one収率 94.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a stirred suspension of sodium hydride (0.9 g, 37.5 mmole) in dimethylformamide (50 mL) was added azocan-2-one (3.83 g, 30 mmole). The mixture was stirred at room temperature for 15 minutes, and then 5-bromo-1-pentene (5.03 g, 33.7 mmole) was added slowly. The reaction mixture was stirred at room temperature for 30 minutes, and then at 80° C. for 16 hours. The solvent was removed under reduced pressure and water was added to the residue. The mixture was extracted with ethyl ether, the organic phase was washed with water, dried (magnesium sulfate) and concentrated to give 1-pent-4-enyl-azocan-2-one (5.53 g,) as an oil.

後処理

  1. stirringThe reaction mixture was stirred at room temperature for 30 minutes
  2. waitat 80° C. for 16 hours
  3. customThe solvent was removed under reduced pressure and water
  4. additionwas added to the residue
  5. extractionThe mixture was extracted with ethyl ether
  6. washthe organic phase was washed with water
  7. dry with materialdried (magnesium sulfate)
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-f9df67df753c4067bb3d87365a9cebae
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07094778B2

反応ノート

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