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Cyclopentanone → Methyl1-[(cyclopentylamino)methyl]cyclopentane-1-carboxylate

HRID 2234511
ノート
印刷プレビュー

反応式

HRID 2234511 の反応式
[CH3:1][O:2][C:3]([C:5]1([CH2:10][NH2:11])[CH2:9][CH2:8][CH2:7][CH2:6]1)=[O:4].[C:12]1(=O)[CH2:16][CH2:15][CH2:14][CH2:13]1.C([O-])(=O)C.[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl>[CH3:1][O:2][C:3]([C:5]1([CH2:10][NH:11][CH:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)[CH2:6][CH2:7][CH2:8][CH2:9]1)=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8452CyclopentanoneHCID 517045Sodium AcetateHCID 5049666Sodium triacetoxyborohydrideHCID 13285792Methyl 1-(aminomethyl)cyclopentanecarboxylate2 回

生成物 1

HCID 68683992Methyl1-[(cyclopentylamino)methyl]cyclopentane-1-carboxylate収率 81%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

Methyl1-(aminomethyl)cyclopentane-1-carboxylate (Intermediate 259; 1.5 g, 9.54 mmol) and cyclopentanone (1.0 mL, 11.45 mmol) were stirred in DCM (40 mL). Sodium acetate (940 mg, 11.45 mmol) and sodium triacetoxyborohydride (3.04 g, 14.31 mmol) were added. The mixture was stirred at room temperature for 48 hours. The reaction mixture was filtered and the filtrate concentrated. The residue was dissolved in methanol and absorbed on to an SCX column, which was then washed with methanol and eluted with ammonia in methanol. Product containing fractions were combined and evaporated to yield the title compound as a colourless oil (1.64 g, 81%).

後処理

  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filtrate concentrated
  3. dissolutionThe residue was dissolved in methanol
  4. customabsorbed on to an SCX column, which
  5. washwas then washed with methanol
  6. washeluted with ammonia in methanol
  7. additionProduct containing fractions
  8. customevaporated

出典と根拠

ORDレコード
ord-e9f0274a85684172b27426ecfdf37dd0
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07709471B2

反応ノート

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