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Dimethylformamide → 2-chloro-4,4-diMethylcyclohex-1-enecarbaldehyde

HRID 573128
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HRID 573128 반응식
CN(C)[CH:3]=[O:4].P(Cl)(Cl)([Cl:8])=O.[CH3:11][C:12]1([CH3:19])[CH2:17][CH2:16][CH2:15][C:14](=O)[CH2:13]1>ClCCl>[Cl:8][C:14]1[CH2:13][C:12]([CH3:19])([CH3:11])[CH2:17][CH2:16][C:15]=1[CH:3]=[O:4]
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 76322Cyclohexanone, 3,3-dimethyl-

생성물 1

HCID 866428722-chloro-4,4-diMethylcyclohex-1-enecarbaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-10 °C

실험 절차

Into a 250 mL round-bottomed flask was added N,N-dimethylformamide (3.5 mL) in dichloromethane (30 mL). The mixture was cooled to −10° C., and phosphoryl trichloride (4 mL) was added dropwise. The solution was warmed up to room temperature and 3,3-dimethylcyclohexanone (5.5 mL) was added slowly. The mixture was heated to reflux overnight. The reaction mixture was quenched with a 0° C. solution of sodium acetate (25 g in 50 mL water). The aqueous layer was extracted with ether (3×200 mL). The organic layers were combined, dried over Na2SO4, filtered, and dried under vacuum to give the title compound.

후처리

  1. temperatureThe solution was warmed up to room temperature
  2. temperatureThe mixture was heated
  3. temperatureto reflux overnight
  4. customThe reaction mixture was quenched with a 0° C. solution of sodium acetate (25 g in 50 mL water)
  5. extractionThe aqueous layer was extracted with ether (3×200 mL)
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. customdried under vacuum

출처 및 근거

ORD 기록
ord-869158c1216c45f6a24093be63d55077
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029404B2

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