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3-Methoxyphenol → 5-Methoxy-2-nitrosophenol

HRID 1655668
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HRID 1655668 반응식
[N:1]([O-:3])=[O:2].[Na+].[CH3:5][O:6][C:7]1[CH:8]=[C:9]([OH:13])[CH:10]=[CH:11][CH:12]=1>O.C(O)(=O)CC>[CH3:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([N:1]=[O:3])=[C:9]([OH:13])[CH:8]=1.[CH3:5][O:6][C:7]1[CH:8]=[C:9]([OH:13])[CH:10]=[CH:11][C:12]=1[N:1]=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 90073-MethoxyphenolHCID 23668193Sodium Nitrite

생성물 2

HCID 838015-Methoxy-2-nitrosophenolHCID 101033473-Methoxy-4-nitrosophenol

시약·촉매·용매 2

HCID 962Water용매HCID 1032Propionic Acid용매

실험 절차

A solution of sodium nitrite (6.9 g, 0.1 mol) dissolved in 15 mL water was added, dropwise, to a solution of 3-methoxyphenol (12.4 g, 0.1 mol) dissolved in propionic acid (100 mL) cooled to -5° to 0° C., at a rate which maintained a temperature of -5° to 0° C. The mixture was stirred for 1 hour to produce a slurry of alkoxy nitrosophenols having a mole ratio of 5-methoxy-2-nitrosophenol to 3-methoxy-4-nitrosophenol of 95:5. Water (85 mL) was added to the slurry and the product was collected by filtration, washed with 60 mL of 50% aqueous propionic acid and then dried to give 10.1 g (66% of theory) of 5-methoxy-2-nitrosophenol which contained approximately 2% of the 3-methoxy-4-nitrosophenol isomer.

후처리

  1. additionwas added
  2. temperaturecooled to -5° to 0° C., at a rate which
  3. temperaturemaintained a temperature of -5° to 0° C

출처 및 근거

ORD 기록
ord-310b659c16f74548b3221ada48a86132
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05250741

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