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Potassium Carbonate → Cyclopropyl-(3-ethynyl-benzyl)-methyl-amine

HRID 1765798
ノート
印刷プレビュー

反応式

HRID 1765798 の反応式
[CH:1]1([N:4]([CH3:18])[CH2:5][C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([C:12]#[C:13][Si](C)(C)C)[CH:7]=2)[CH2:3][CH2:2]1.C(=O)([O-])[O-].[K+].[K+]>CO>[CH:1]1([N:4]([CH2:5][C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([C:12]#[CH:13])[CH:7]=2)[CH3:18])[CH2:3][CH2:2]1
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 11430Potassium CarbonateHCID 57424247Cyclopropyl-methyl-(3-trimethylsilanylethynyl-benzyl)-amine2 回

生成物 1

HCID 21107260Cyclopropyl-(3-ethynyl-benzyl)-methyl-amine収率 86%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution cyclopropyl-methyl-(3-trimethylsilanylethynyl-benzyl)-amine (Intermediate 90, 0.355 g, 1.38 mmol) in methanol (10 mL) was treated with potassium carbonate (0.13 g, 0.95 mmol) and the resulting reaction mixture was stirred at ambient temperature overnight. The solvent was evaporated in vacuo, the residue was diluted with water and extracted with diethyl ether. The organic phase was washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title compound (0.22 g, 86%).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customthe resulting reaction mixture
  2. customThe solvent was evaporated in vacuo
  3. additionthe residue was diluted with water
  4. extractionextracted with diethyl ether
  5. washThe organic phase was washed with brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customevaporated in vacuo

出典と根拠

ORDレコード
ord-467a99a202b04670b2dae624782029bc
出典データセット
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07226951B2

反応ノート

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