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Hydrochloric Acid → Methyl 2-hydroxy-4-isopropoxybenzoate

HRID 2293537
ノート
印刷プレビュー

反応式

HRID 2293537 の反応式
[OH:1][C:2]1[CH:11]=[C:10]([OH:12])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].C(=O)([O-])[O-].[K+].[K+].[CH:19](I)([CH3:21])[CH3:20].Cl>CC(C)=O>[OH:1][C:2]1[CH:11]=[C:10]([O:12][CH:19]([CH3:21])[CH3:20])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 6362Isopropyl iodideHCID 11430Potassium CarbonateHCID 16523Methyl 2,4-Dihydroxybenzoate

生成物 1

HCID 23244891Methyl 2-hydroxy-4-isopropoxybenzoate

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A 1.50 g portion of methyl 2,4-dihydroxybenzoate was dissolved in 30 ml of acetone, and 3.10 g of potassium carbonate and 1.7 ml of isopropyl iodide were added, followed by 48 hours of heating under reflux. After completion of the reaction, the reaction solution was poured into 1N hydrochloric acid aqueous solution, extracted with chloroform and dried over anhydrous sodium sulfate and then the solvent was evaporated under a reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1-2:1) to give 1.60 g of methyl 2-hydroxy-4-isopropoxybenzoate.

後処理

  1. temperatureof heating
  2. temperatureunder reflux
  3. customAfter completion of the reaction
  4. extractionextracted with chloroform
  5. dry with materialdried over anhydrous sodium sulfate
  6. customthe solvent was evaporated under a reduced pressure
  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-33be7e034ca845a8b610442816256930
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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