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Dimethyl Sulfate → Methyl 4-isopropoxy-2-methoxybenzoate

HRID 2293538
ノート
印刷プレビュー

反応式

HRID 2293538 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 21477058Methyl 4-isopropoxy-2-methoxybenzoate

試薬・触媒・溶媒 1

HCID 6569Methyl Ethyl Ketone溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-af0a816398bb4f319ccbe8b9160c84b4
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05686482

反応ノート

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