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

HRID 468516
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HRID 468516 반응식
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]
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참가 물질

5

반응물 2

HCID 24819Phosphorus pentachlorideHCID 96925Methyl 2,2-dimethylacetoacetate

생성물 1

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

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-24784b6827944374817aaa51baefcbe5
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08623905B2

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