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Sodium bis(2-methoxyethoxy)aluminiumhydride → 1,2,2a,3,4,5-Hexahydroacenaphthylen-1-amine

HRID 331230
ノート
印刷プレビュー

反応式

HRID 331230 の反応式
[C:1]1(=[N:13]O)[C:11]2=[C:12]3[C:7](=[CH:8][CH:9]=[CH:10]2)[CH2:6][CH2:5][CH2:4][CH:3]3[CH2:2]1.[H-].[H-].COCCO[Al+]OCCOC.[Na+]>C1(C)C=CC=CC=1>[CH:1]1([NH2:13])[C:11]2=[C:12]3[C:7](=[CH:8][CH:9]=[CH:10]2)[CH2:6][CH2:5][CH2:4][CH:3]3[CH2:2]1
参加物反応条件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 21584525Sodium bis(2-methoxyethoxy)aluminiumhydrideHCID 866416292a,3,4,5-tetrahydro-2H-acenaphthylen-1-one oxime

生成物 1

HCID 638213741,2,2a,3,4,5-Hexahydroacenaphthylen-1-amine収率 83%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
80 °C

実験手順

To 2a,3,4,5-tetrahydro-2H-acenaphthylen-1-one oxime (7.00 g) was added a solution (about 65%, 50 ml) of sodium bis(2-methoxyethoxy)aluminum dihydride in toluene, and the mixture was stirred with heating at 80° C. for 2 hr. After cooling to room temperature, the reaction mixture was poured into ice water, and the mixture was extracted with chloroform. After concentration under reduced pressure, the residue was extracted with 1N hydrochloric acid. The aqueous layer was alkalified with potassium carbonate, and extracted with chloroform. The extract was washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure to give the title compound (5.34 g, 83%).

後処理

  1. temperatureAfter cooling to room temperature
  2. extractionthe mixture was extracted with chloroform
  3. concentrationAfter concentration under reduced pressure
  4. extractionthe residue was extracted with 1N hydrochloric acid
  5. extractionextracted with chloroform
  6. washThe extract was washed with saturated brine
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-691ab29fc7484478b86179744f67ea7d
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08877779B2

反応ノート

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