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

HRID 503357
ノート
印刷プレビュー

反応式

HRID 503357 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]>C(Cl)Cl.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収率 38.6%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide触媒HCID 6344Dichloromethane溶媒

実験手順

To a suspension of PCl5 (270 g, 1.3 mol) in CH2Cl2 (1000 mL) was added dropwise methyl 2,2-dimethyl-3-oxobutanoate (85 g) at 0° C., following by addition of approximately 30 drops of dry DMF. The mixture was heated at reflux overnight. The reaction mixture was cooled to ambient temperature and slowly poured into ice water. The organic layer was separated and the aqueous phase was extracted with CH2Cl2 (500 mL×3). The combined organic layers were washed with saturated aqueous NaHCO3 and dried over anhydrous Na2SO4. The solvent was evaporated and the residue was distilled under reduced pressure to give methyl 3-chloro-2,2-dimethylbut-3-enoate (37 g, 23%). 1H NMR (400 MHz, CDCl3) δ 5.33 (s, 1H), 3.73 (s, 3H), 1.44 (s, 6H).

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux overnight
  3. customThe organic layer was separated
  4. extractionthe aqueous phase was extracted with CH2Cl2 (500 mL×3)
  5. washThe combined organic layers were washed with saturated aqueous NaHCO3
  6. dry with materialdried over anhydrous Na2SO4
  7. customThe solvent was evaporated
  8. distillationthe residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-e3d20f40867e47b09524956519fb4366
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07776905B2

反応ノート

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