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Hydrochloric Acid → 1-(2-Fluoro-4,6-dimethoxyphenyl)propane-1-one

HRID 601654
ノート
印刷プレビュー

反応式

HRID 601654 の反応式
ClC(Cl)C.[CH3:5][O:6][C:7]1[CH:8]=[C:9]([F:15])[CH:10]=[C:11]([O:13][CH3:14])[CH:12]=1.[C:16](Cl)(=[O:19])[CH2:17][CH3:18].Cl>[Cl-].[Cl-].[Zn+2]>[F:15][C:9]1[CH:8]=[C:7]([O:6][CH3:5])[CH:12]=[C:11]([O:13][CH3:14])[C:10]=1[C:16](=[O:19])[CH2:17][CH3:18]
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 63651,1-Dichloroethane3 回HCID 62324Propionyl chlorideHCID 27742571-Fluoro-3,5-dimethoxybenzene

生成物 1

HCID 231582391-(2-Fluoro-4,6-dimethoxyphenyl)propane-1-one収率 50,306.301%

試薬・触媒・溶媒 1

HCID 3007855Zincchloride
触媒

実験手順

Under nitrogen atmosphere, 5 ml solution of dichloroethane with 2 g of 3,5-dimethoxy-1-fluorobenzene, and 5 ml solution of dichloroethane with 1.3 mg of propionyl chloride were dropped sequentiallly at −10° C. to 40 ml solution of dichloroethane with 2.4 g of alumimium trichloride and 240 mg of zinc dichloride, and the mixture was stirred at room temperature for 2 hours. 20% hydrochloric acid aqueous solution was added to the reaction solution, extracted with chloroform. Chloroform layer was washed with saturated saline solution, dried with anhydrous sodium sulfate. The solvents were distilled outunder reduced pressure and the residues were separated and purified by silicagel chromatography (hexane/ethyl acetate=5/1), to obtain 1.5 g of the above compound as a white solid.

後処理

  1. extractionextracted with chloroform
  2. washChloroform layer was washed with saturated saline solution
  3. dry with materialdried with anhydrous sodium sulfate
  4. distillationThe solvents were distilled outunder reduced pressure
  5. customthe residues were separated
  6. custompurified by silicagel chromatography (hexane/ethyl acetate=5/1)

出典と根拠

ORDレコード
ord-d5fe795567fc4587aca9f1869ce9b2bc
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07902369B2

反応ノート

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