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N-phenethyl-N-propyl-3,4-dimethoxyphenethylamine → 4-{2-[(2-Phenylethyl)(propyl)amino]ethyl}benzene-1,2-diol

HRID 46776
ノート
印刷プレビュー

反応式

HRID 46776 の反応式
[CH2:1]([N:9]([CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21]C)=[C:17]([O:23]C)[CH:16]=1)[CH2:10][CH2:11][CH3:12])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>Br>[CH2:1]([N:9]([CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([OH:21])=[C:17]([OH:23])[CH:16]=1)[CH2:10][CH2:11][CH3:12])[CH2:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH: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

3

反応物 1

HCID 12411034N-phenethyl-N-propyl-3,4-dimethoxyphenethylamine

生成物 1

HCID 30486884-{2-[(2-Phenylethyl)(propyl)amino]ethyl}benzene-1,2-diol収率 94.5%

試薬・触媒・溶媒 1

HCID 260Hydrogen Bromide溶媒

実験手順

A solution of 9.37 g of the product of Step B in 90 ml of 48% hydrobromic acid was refluxed for 3 hours under a nitrogen atmosphere and was then evaporated to dryness. The residue was taken up in 50 ml of ammonium hydroxide solution and the solution was extracted with methylene chloride. The organic extracts were washed with water, dried over magnesium sulfate, filtered and evaporated to dryness to obtain 8.1 g of N-phenethyl-N-propyl-3,4-dihydroxyphenethylamine in the form of a reddish oil.

後処理

custom
was then evaporated to dryness
  • extractionthe solution was extracted with methylene chloride
  • washThe organic extracts were washed with water
  • dry with materialdried over magnesium sulfate
  • filtrationfiltered
  • customevaporated to dryness
  • 出典と根拠

    ORDレコード
    ord-e7aca4c10bec4b2c820e51a605cbb214
    出典データセット
    uspto-grants-1979_11
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04175136

    反応ノート

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