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Dimethyl Sulfoxide → 1-Cyclopropanecarbonylpiperidin-4-one

HRID 374806
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HRID 374806 반응식
[C:1](Cl)(=[O:5])[C:2](Cl)=O.CS(C)=[O:9].[CH2:11]([N:13]([CH2:16][CH3:17])[CH2:14][CH3:15])C.Cl[CH:19](Cl)[CH3:20]>ClCCl>[CH:15]1([C:14]([N:13]2[CH2:11][CH2:2][C:1](=[O:5])[CH2:17][CH2:16]2)=[O:9])[CH2:20][CH2:19]1
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참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 63651,1-DichloroethaneHCID 8471TriethylamineHCID 65578Oxalyl chloride

생성물 1

HCID 149949681-Cyclopropanecarbonylpiperidin-4-one수율 76%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

66 g of oxalic chloride was dissolved in 500 ml of dichloroethane, into which 61 g of dimethyl sulfoxide was gradually dropped at -67° C. 44 g of 1-cycloprpanecarbonyl-4-hydroxypiperidine dissolved in 200 ml of dichloromethane was dropped into the above solution at -67° C. At -67° C. 131 g of triethylamine was further added, followed by returning to room temperature. The resultant salt was removed by filtration and the filtrate was once concentrated, after which water was added to the concentrate, followed by extraction with ethyl acetate and drying with anhydrous magnesium sulfate. Moreover, the aqueous phase was extracted with chloroform and dried similarly. The solvent was distilled off under reduced pressure and the resultant residue was purified by the use of silica gel column chromatography (elution solvent: ethyl acetate:hexane=3:7), thereby obtaining 33 g of the intended compound (yield 76%).

후처리

  1. additionwas gradually dropped at -67° C
  2. additionwas dropped into the above solution at -67° C
  3. customAt -67° C
  4. customby returning to room temperature
  5. customThe resultant salt was removed by filtration
  6. concentrationthe filtrate was once concentrated
  7. additionafter which water was added to the concentrate
  8. extractionfollowed by extraction with ethyl acetate
  9. dry with materialdrying with anhydrous magnesium sulfate
  10. extractionMoreover, the aqueous phase was extracted with chloroform
  11. customdried similarly
  12. distillationThe solvent was distilled off under reduced pressure
  13. customthe resultant residue was purified by the use of silica gel column chromatography (elution solvent: ethyl acetate:hexane=3:7)

출처 및 근거

ORD 기록
ord-300bbf56630e4d1f99f5080f5dabb886
출처 데이터셋
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05482937

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