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Styrene Oxide → 2-((3,4-Dimethoxybenzyl)amino)-1-phenylethanol

HRID 2255043
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인쇄 미리보기

반응식

HRID 2255043 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH2:6][NH2:7].[CH2:13]1[O:21][CH:14]1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(#N)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH2:6][NH:7][CH2:13][CH:14]([OH:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7276Styrene OxideHCID 79832Veratrylamine

생성물 1

HCID 47199872-((3,4-Dimethoxybenzyl)amino)-1-phenylethanol수율 46.7%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Heat a solution of 3,4-dimethoxybenzylamine (16.7 g) and styrene oxide (12.0 g) in acetonitrile (250 mL) at reflux for 16 h. Concentrate to a residue and distill the residue, collecting the fraction distilling above 120° C. (0.5 mm). Recrystallize the solidified distillate from benzene/hexane to give N-(3,4-dimethoxybenzyl)-2-hydroxy-2-phenylethylamine (13.4 g), mp=93°-94° C.

후처리

  1. temperatureat reflux for 16 h
  2. concentrationConcentrate to a residue
  3. distillationdistill the residue
  4. customcollecting the fraction
  5. distillationdistilling above 120° C. (0.5 mm)
  6. customRecrystallize the solidified distillate from benzene/hexane

출처 및 근거

ORD 기록
ord-fb2e33c1808944a5ba2dc2c5542a5e11
출처 데이터셋
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05238935

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