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Methyl iodide → 1,3-Dichloro-4-methoxy-2-nitrobenzene

HRID 1771678
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HRID 1771678 반응식
[Cl:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[C:6]([Cl:11])[CH:5]=[CH:4][C:3]=1[OH:12].[C:13]([O-])([O-])=O.[K+].[K+].CI>CC(C)=O>[Cl:11][C:6]1[CH:5]=[CH:4][C:3]([O:12][CH3:13])=[C:2]([Cl:1])[C:7]=1[N+:8]([O-:10])=[O:9]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 205139322,4-Dichloro-3-nitrophenol

생성물 1

HCID 205138861,3-Dichloro-4-methoxy-2-nitrobenzene수율 86%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution of 2,4-dichloro-3-nitro-phenol (600 mg, 2.9 mmol, 1.0 eq) in acetone (30 mL), was added K2CO3 (1.2 g, 8.7 mmol, 3.0 eq) and the solution was stirred at room temperature for 30 min. Methyl iodide (1.2 g, 8.7 mmol, 3.0 eq) was added and the reaction was stirred at room temperature overnight. The reaction was filtered to remove the inorganic salts and the organic phase was evaporated in vacuo to give the title compound (550 mg, 86%).

후처리

  1. stirringthe reaction was stirred at room temperature overnight
  2. filtrationThe reaction was filtered
  3. customto remove the inorganic salts
  4. customthe organic phase was evaporated in vacuo

출처 및 근거

ORD 기록
ord-7074dac009fa46b0a988e9fe93fd5563
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249085B2

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