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1,4-Dibenzyl-2-(methoxymethyl)piperazine → 2-(Methoxymethyl)piperazine

HRID 16873
ノート
印刷プレビュー

反応式

HRID 16873 の反応式
C([N:8]1[CH2:13][CH2:12][N:11](CC2C=CC=CC=2)[CH2:10][CH:9]1[CH2:21][O:22][CH3:23])C1C=CC=CC=1>C(O)C.[Pd]>[CH3:23][O:22][CH2:21][CH:9]1[CH2:10][NH:11][CH2:12][CH2:13][NH:8]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 1

HCID 197635561,4-Dibenzyl-2-(methoxymethyl)piperazine

生成物 1

HCID 142302642-(Methoxymethyl)piperazine収率 84.5%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

1,4-Dibenzyl-2-(methoxymethyl)piperazine (1.578 g, 5.08 mmol) and palladium (10% on carbon, 0.163 g, 1.53 mmol) in ethanol (50.8 ml) were stirred under an atmosphere of hydrogen at room temperature for 3 days. The reaction mixture was filtered through celite, washing with ethanol. The resulting mixture was evaporated to dryness to afford crude product. The crude product was purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH and fractions were evaporated to dryness to afford 2-(methoxymethyl)piperazine (0.559 g, 84%) as a yellow oil. This was used directly without further purification.

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. filtrationThe reaction mixture was filtered through celite
  2. washwashing with ethanol
  3. customThe resulting mixture was evaporated to dryness
  4. customto afford crude product
  5. customThe crude product was purified by ion exchange chromatography
  6. washThe desired product was eluted from the column
  7. customwere evaporated to dryness

出典と根拠

ORDレコード
ord-a5d6aecb5220441a957e5d9325a888d1
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07737149B2

反応ノート

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