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2',4'-Dihydroxyacetophenone → 1-(2-Hydroxy-4-(methoxymethoxy)phenyl)ethanone

HRID 1030685
ノート
印刷プレビュー

反応式

HRID 1030685 の反応式
[OH:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10].C(N(CC)C(C)C)(C)C.[CH3:21][O:22][CH2:23]Cl>CN(C)C=O>[OH:1][C:2]1[CH:7]=[C:6]([O:8][CH2:21][O:22][CH3:23])[CH:5]=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10]
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 69902',4'-DihydroxyacetophenoneHCID 7864Chloromethyl Methyl EtherHCID 81531Diisopropylethylamine

生成物 1

HCID 117455591-(2-Hydroxy-4-(methoxymethoxy)phenyl)ethanone収率 87.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

In 60 ml of dimethylformamide were dissolved 5.0 g of 2',4'-dihydroxyacetophenone and 6.37 g of N,N-diisopropylethylamine, and 2.72 ml of chloromethyl methyl ether was gradually added to the solution under ice cooling. The mixture was stirred under ice cooling for 20 minutes and a reaction was carried out at room temperature for 1.5 hours. After the reaction, the reaction mixture was extracted with 300 ml of diethyl ether, and the diethyl ether layer was washed with water (100 ml×2 times), shaken with a saturated aqueous solution of sodium chloride (50 ml×2 times), dried with anhydrous sodium sulfate and filtered. The solvent was removed from the filtrate by distillation and the residue was subjected to the silica gel chromatography (3.5 cm in diameter; 72.8 g; n-hexane/ethyl acetate=4/1; 0.3 kg/cm2) to obtain 5.66 g (yield=87.8%) of 2'-hydroxy-4'-methoxymethoxyacetophenone in the form of a colorless oil.

後処理

  1. additionwas gradually added to the solution under ice cooling
  2. waita reaction was carried out at room temperature for 1.5 hours
  3. customAfter the reaction
  4. extractionthe reaction mixture was extracted with 300 ml of diethyl ether
  5. washthe diethyl ether layer was washed with water (100 ml×2 times)
  6. stirringshaken with a saturated aqueous solution of sodium chloride (50 ml×2 times)
  7. dry with materialdried with anhydrous sodium sulfate
  8. filtrationfiltered
  9. customThe solvent was removed from the filtrate by distillation

出典と根拠

ORDレコード
ord-c045d53ceac64f858aca84b1b7a6c8a9
出典データセット
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05106871

反応ノート

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