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Sodium Hydroxide → 3-[2-(N,N-Dimethylamino)ethyl]-1,2,3,4-tetrahydroquinoline

HRID 2269714
ノート
印刷プレビュー

反応式

HRID 2269714 の反応式
[CH3:1][N:2]([CH3:17])[C:3](=O)[CH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][C:6]1=O.[OH-].[Na+]>Cl>[CH3:1][N:2]([CH2:3][CH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH2:6]1)[CH3:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 10585665N,N-Dimethyl-2-oxo-1,2,3,4-tetrahydro-3-quinolineacetoamide

生成物 1

HCID 183331263-[2-(N,N-Dimethylamino)ethyl]-1,2,3,4-tetrahydroquinoline収率 75.1%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

Borane-THF complex (1M; 15 ml) was added to N,N-dimethyl-2-oxo-1,2,3,4-tetrahydro-3-quinolineacetoamide (590 mg), which was heated under reflux for 3.5 hours. 6N hydrochloric acid (10 ml) was added to the reaction mixture, which was heated under reflux overnight. 6N sodium hydroxide was added to the reaction mixture to adjust pH to 7 and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, then dried and concentrated. The residue was purified by alumina column chromatography (eluent: hexane/ethyl acetate=1/1) to obtain the entitled compound (390 mg) as an oily substance.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 3.5 hours
  3. temperaturewas heated
  4. temperatureunder reflux overnight
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with a saturated aqueous sodium bicarbonate solution
  7. dry with materiala saturated aqueous sodium chloride solution, then dried
  8. concentrationconcentrated
  9. customThe residue was purified by alumina column chromatography (eluent: hexane/ethyl acetate=1/1)

出典と根拠

ORDレコード
ord-5e6b2901d14c47e4aba22c49b92f3992
出典データセット
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06329389B1

反応ノート

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