Ethanol → Ethyl-4-(3-fluoro-2-methoxyphenyl)-2-oxo-4-methyl-valerate

HRID 1869312ノート

反応式

HRID 1869312 の反応式
[F:1][C:2]1[C:3]([O:17][CH3:18])=[C:4]([C:8]([CH3:16])([CH3:15])[CH2:9][C:10](=[O:14])[C:11]([OH:13])=[O:12])[CH:5]=[CH:6][CH:7]=1.S(=O)(=O)(O)O.[CH2:24](O)[CH3:25]>>[CH2:24]([O:12][C:11](=[O:13])[C:10](=[O:14])[CH2:9][C:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[C:3]=1[O:17][CH3:18])([CH3:16])[CH3:15])[CH3:25]

参加物

4

反応物 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 179890854-(3-Fluoro-2-methoxyphenyl)-4-methyl-2-oxo-pentanoic acid

生成物 1

HCID 17989088Ethyl-4-(3-fluoro-2-methoxyphenyl)-2-oxo-4-methyl-valerate収率 90.6%

実験手順

4.14 g (16.28 mmol) of 4-(3-fluoro-2-methoxyphenyl)-4-methyl-2-oxo-pentanoic acid is dissolved in 97 ml of ethanol, mixed with 1.79 ml of sulfuric acid and refluxed for four hours. The ethanol is drawn off in a rotary evaporator, and the residue is carefully mixed with saturated sodium bicarbonate solution until a pH of 9 is reached. It is extracted twice with 100 ml each of ethyl acetate, and the combined organic extracts are washed with water and then with brine. After the desiccant is dried and filtered off, and after the solvent is spun in, the residue is chromatographed on silica gel (mobile solvent ethyl acetate/hexane). 4.16 g (90.6%) of the desired compound is isolated.

後処理

  1. temperaturerefluxed for four hours
  2. customThe ethanol is drawn off in a rotary evaporator
  3. additionthe residue is carefully mixed with saturated sodium bicarbonate solution until a pH of 9
  4. extractionIt is extracted twice with 100 ml each of ethyl acetate
  5. washthe combined organic extracts are washed with water
  6. customAfter the desiccant is dried
  7. filtrationfiltered off
  8. customis chromatographed on silica gel (mobile solvent ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-9bb8ac77ffb64b6f9d51e83e80f56bf5
出典データセット
uspto-grants-2009_12
特許番号
US07638515B2

反応ノート

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