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Methyl iodide → 4-(Allyloxy)-2-methoxy-1-(methylsulfanyl)benzene

HRID 724269
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HRID 724269 반응식
[CH2:1]([O:4][C:5]1[CH:6]=[CH:7][C:8]([SH:12])=[C:9](O)[CH:10]=1)[CH:2]=[CH2:3].[C:13](=[O:16])([O-])[O-].[K+].[K+].[CH3:19]I>CC(C)=O>[CH2:1]([O:4][C:5]1[CH:6]=[CH:7][C:8]([S:12][CH3:19])=[C:9]([O:16][CH3:13])[CH:10]=1)[CH:2]=[CH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 218771835-(Allyloxy)-2-sulfanylphenol

생성물 1

HCID 218771484-(Allyloxy)-2-methoxy-1-(methylsulfanyl)benzene

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

5-(Allyloxy)-2-sulfanylphenol (37.84 g, 0.21 mol) and potassium carbonate (43 g, 0.31 mol) in acetone (450 ml) was cooled to 5° C. and treated with methyl iodide (32.32 ml, 0.52 mol) dropwise and stirred for 1 h at RT. After removal of the solvent in vacuo, the residue was partioned between diethyl ether (300 ml) and water (400 ml). The aqueous phase was separated and extracted with further diethyl ether (2×150 ml) and the combined organics were dried over MgSO4 and evaporated to a clear oil (26 g, 0.12 mol).

후처리

  1. customAfter removal of the solvent in vacuo
  2. customThe aqueous phase was separated
  3. extractionextracted with further diethyl ether (2×150 ml)
  4. dry with materialthe combined organics were dried over MgSO4

출처 및 근거

ORD 기록
ord-4a589f2b4250443392094a9983cb5293
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07141586B2

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