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

HRID 46776
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인쇄 미리보기

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HRID 46776 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

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

생성물 1

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

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

실험 절차

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.

후처리

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
  • 출처 및 근거

    ORD 기록
    ord-e7aca4c10bec4b2c820e51a605cbb214
    출처 데이터셋
    uspto-grants-1979_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04175136

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