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Toluene → (1S)-1-Benzyl-2-(dimethylamino) Ethylamine

HRID 1879466
ノート
印刷プレビュー

反応式

HRID 1879466 の反応式
[NH2:1][C@@H:2]([CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:3]([N:5]([CH3:7])[CH3:6])=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].C1(C)C=CC=CC=1.CCOCC>O1CCCC1.C(OCC)(=O)C>[CH3:7][N:5]([CH3:6])[CH2:3][C@@H:2]([NH2:1])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 1140TolueneHCID 3283Diethyl EtherHCID 11008771(S)-2-amino-N,N-dimethyl-3-phenylpropanamideHCID 21226445Aluminium lithium hydride2 回

生成物 1

HCID 11251722(1S)-1-Benzyl-2-(dimethylamino) Ethylamine収率 65%

試薬・触媒・溶媒 2

HCID 8028
Tetrahydrofuran
溶媒
2 回
HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of (S)-2-amino-N,N-dimethyl-3-phenyl-propionamide (1.0 g, 5.2 mmol) in tetrahydrofuran (10 mL) was added a solution of lithium aluminum hydride in tetrahydrofuran and toluene (3.5 M, 7.4 mL, 26 mmol) dropwise. The mixture was heated to reflux for 4 h after addition and then cooled. Ether (20 mL) was added. Ethyl acetate was added dropwise until all the lithium aluminum hydride was consumed. Sodium hydroxide (1M, 20 mL) was added and the mixture was stirred for 30 min. The mixture was extracted three times with ether. The combined organic extracts were washed with brine, dried over sodium sulfate and evaporated to give (S)—N1,N1-dimethyl-3-phenyl-propane-1,2-diamine (0.60 g, 65%)

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 4 h
  3. additionafter addition
  4. temperaturecooled
  5. customwas consumed
  6. additionSodium hydroxide (1M, 20 mL) was added
  7. extractionThe mixture was extracted three times with ether
  8. washThe combined organic extracts were washed with brine
  9. dry with materialdried over sodium sulfate
  10. customevaporated

出典と根拠

ORDレコード
ord-36d5ee014ca64321aa6d9466f68f8a8c
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08314250B2

反応ノート

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