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Dimethyl Sulfate → Methyl 4-isopropoxy-2-methoxybenzoate

HRID 2293538
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HRID 2293538 반응식
[OH:1][C:2]1[CH:11]=[C:10]([O:12][CH:13]([CH3:15])[CH3:14])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[C:16](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CC(=O)CC>[CH:13]([O:12][C:10]1[CH:9]=[CH:8][C:3]([C:4]([O:6][CH3:7])=[O:5])=[C:2]([O:1][CH3:16])[CH:11]=1)([CH3:15])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 23244891Methyl 2-hydroxy-4-isopropoxybenzoate

생성물 1

HCID 21477058Methyl 4-isopropoxy-2-methoxybenzoate

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

A 1.60 g portion of methyl 2-hydroxy-4-isopropoxybenzoate was dissolved in 30 ml of 2-butanone, 1.60 g of potassium carbonate and 1.1 ml of dimethyl sulfate were added, followed by 12 hours of heating under reflux. After completion of the reaction, the solvent was evaporated, the resulting residue was suspended in chloroform, insoluble matter was removed by filtration through celite, and the solvent was again evaporated. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1-2:1) to give 1.70 g of methyl 4-isopropoxy-2-methoxybenzoate.

후처리

  1. temperatureof heating
  2. temperatureunder reflux
  3. customAfter completion of the reaction
  4. customthe solvent was evaporated
  5. custominsoluble matter was removed by filtration through celite
  6. customthe solvent was again evaporated
  7. customThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1-2:1)

출처 및 근거

ORD 기록
ord-af0a816398bb4f319ccbe8b9160c84b4
출처 데이터셋
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05686482

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