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

HRID 1036002
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HRID 1036002 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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

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

반응 조건

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 by 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.

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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 by 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-0f31948192444f2bb19fa99d93a0718f
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546399B2

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