Propargyl bromide → (2-Methoxyethyl)(methyl)(prop-2-yn-1-yl)amine

HRID 276824

反応式

HRID 276824 の反応式
[CH2:1](Br)[C:2]#[CH:3].[CH3:5][O:6][CH2:7][CH2:8][NH:9][CH3:10].C(=O)([O-])[O-].[Cs+].[Cs+]>CC(C)=O>[CH3:5][O:6][CH2:7][CH2:8][N:9]([CH3:10])[CH2:1][C:2]#[CH:3]

参加物

5

反応物 3

HCID 7842Propargyl bromideHCID 10796Cesium carbonateHCID 300977(2-Methoxyethyl)(methyl)amine

生成物 1

HCID 18548974(2-Methoxyethyl)(methyl)(prop-2-yn-1-yl)amine収率 48.9%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

Propargyl bromide (26.8 g, 225 mmol) was added dropwise to a mixture of N-(2-methoxyethyl)methyl amine (20 g, 225 mmol) and cesium carbonate (73 g, 225 mmol) in 350 mL of acetone. The mixture was stirred overnight under nitrogen at room temperature. The inorganic salts were then filtered off, and the solvent was removed. The residue was dissolved in saturated sodium bicarbonate solution and extracted with ethyl acetate. The organic extracts were then evaporated to give 14 g of (2-methoxy-ethyl)-methyl-prop-2-ynyl-amine: mass spectrum (m/e): M+H 127.

後処理

  1. filtrationThe inorganic salts were then filtered off
  2. customthe solvent was removed
  3. dissolutionThe residue was dissolved in saturated sodium bicarbonate solution
  4. extractionextracted with ethyl acetate
  5. customThe organic extracts were then evaporated

出典と根拠

ORDレコード
ord-b3357c4a48654098b12a96e430fda5fa
出典データセット
uspto-grants-2002_03
特許番号
US06355636B1

関連ノート

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