Sodium hydride → 2-Acetyl-2-fluoro-6-(trimethylsilyl)-5-hexynoic acid ethyl ester

HRID 67185ノート

反応式

HRID 67185 の反応式
[CH2:1]([O:3][C:4](=[O:17])[CH:5]([C:14](=[O:16])[CH3:15])[CH2:6][CH2:7][C:8]#[C:9][Si:10]([CH3:13])([CH3:12])[CH3:11])[CH3:2].[H-].[Na+].Cl([F:24])(=O)(=O)=O>C1(C)C=CC=CC=1>[CH2:1]([O:3][C:4](=[O:17])[C:5]([C:14](=[O:16])[CH3:15])([F:24])[CH2:6][CH2:7][C:8]#[C:9][Si:10]([CH3:11])([CH3:13])[CH3:12])[CH3:2]

参加物

4

実験手順

2-acetyl-6-(trimethylsilyl)-5-hexynoic acid ethyl ester (7.1 g) was added to a suspension of sodium hydride (1.0 g) in toluene under a positive argon atmosphere. After stirring for 1 hour, the reaction mixture was cooled to -10° and a mixture of perchloryl fluoride and argon gases was bubbled through the reaction mixture at such a rate that the internal temperature never exceeded 0° C. The perchloryl fluoride addition was discontinued when it ceased to be exothermic. Argon was bubbled through the mixture as it was allowed to warm to room temperature. The reaction mixture was partitioned between hexane and water and the organic phase was dried (MgSO4) and condensed by rotary evaporation to give an oil. The components of the oil were separated by silica gel chromatography using 30% ethyl acetate/hexane as the eluant to give 5.9 g of 2-acetyl-2-fluoro-6-(trimethylsilyl)-5-hexynoic acid ethyl ester. There was also obtained 0.25 g of 2-fluoro-6-(trimethylsilyl)-5-hexynoic acid ethyl ester.

後処理

  1. temperaturethe reaction mixture was cooled to -10°
  2. customwas bubbled through the reaction mixture at such a rate that the internal temperature never exceeded 0° C
  3. additionThe perchloryl fluoride addition
  4. customArgon was bubbled through the mixture as it
  5. customThe reaction mixture was partitioned between hexane and water
  6. customthe organic phase was dried
  7. custom(MgSO4) and condensed
  8. customby rotary evaporation
  9. customto give an oil
  10. customThe components of the oil were separated by silica gel chromatography

出典と根拠

ORDレコード
ord-e6427a8cf1cb4a8b989b5e628473b81b
出典データセット
uspto-grants-1982_08
特許番号
US04345084

反応ノート

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