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Phosphorus pentachloride → Methyl 3-chloro-2,2-dimethylbut-3-enoate

HRID 468516
ノート
印刷プレビュー

反応式

HRID 468516 の反応式
P(Cl)(Cl)(Cl)(Cl)[Cl:2].[CH3:7][C:8]([CH3:16])([C:13](=O)[CH3:14])[C:9]([O:11][CH3:12])=[O:10]>ClCCl.CN(C=O)C>[Cl:2][C:13](=[CH2:14])[C:8]([CH3:16])([CH3:7])[C:9]([O:11][CH3:12])=[O: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 2

HCID 24819Phosphorus pentachlorideHCID 96925Methyl 2,2-dimethylacetoacetate

生成物 1

HCID 40423475Methyl 3-chloro-2,2-dimethylbut-3-enoate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide触媒HCID 6344Dichloromethane溶媒

実験手順

To a suspension of PCl5 (161 g, 0.772 mol) in dichloromethane (600 mL) was added dropwise methyl 2,2-dimethyl-3-oxobutanoate (52 g, 0.361 mol, crude from last step) at 0° C., followed by the addition of approximately 20 drops of dry DMF. The mixture was heated at reflux overnight. After cooling, the reaction mixture was slowly poured into ice water. The organic layer was separated and the aqueous phase was extracted with dichloromethane (300 mL×3). The combined organic layers were washed with saturated aqueous NaHCO3 solution and dried over anhydrous Na2SO4. The solvent was evaporated to give the product, methyl 3-chloro-2,2-dimethylbut-3-enoate which was used without further purification (47 g, 82%).

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux overnight
  3. temperatureAfter cooling
  4. customThe organic layer was separated
  5. extractionthe aqueous phase was extracted with dichloromethane (300 mL×3)
  6. washThe combined organic layers were washed with saturated aqueous NaHCO3 solution
  7. dry with materialdried over anhydrous Na2SO4
  8. customThe solvent was evaporated

出典と根拠

ORDレコード
ord-24784b6827944374817aaa51baefcbe5
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08623905B2

反応ノート

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