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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethylformamide → 2-Chloro-4,4-dimethylcyclopent-1-enecarbaldehyde

HRID 519402
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HRID 519402 반응식
CN([CH:4]=[O:5])C.O=P(Cl)(Cl)[Cl:8].[CH3:11][C:12]1([CH3:18])[CH2:16][CH2:15][C:14](=O)[CH2:13]1.C([O-])(=O)C.[Na+]>ClCCl>[Cl:8][C:14]1[CH2:13][C:12]([CH3:18])([CH3:11])[CH2:16][C:15]=1[CH:4]=[O:5]
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참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 517045Sodium AcetateHCID 6431023,3-Dimethylcyclopentan-1-one

생성물 1

HCID 866612412-Chloro-4,4-dimethylcyclopent-1-enecarbaldehyde수율 83.2%

시약·촉매·용매 1

HCID 6344Dichloromethane
용매

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온도
20 °C

실험 절차

To a solution of DMF (18.3 g, 250 mmol) in dichloromethane (300 mL) cooled at 0° C. was added POCl3 (40.5 g, 250 mmol) over a period of 10 minutes. See FIG. 15. The mixture was stirred at 20° C. for 1 h. To the above mixture was added 131a (28.0 g, 250 mmol) dropwise over a period of 20 minutes. The resulting mixture was heated at reflux for 20 h. The reaction mixture was cooled to room temperature and poured into a solution of sodium acetate (60 g) in ice-water (400 g). The mixture was extracted with dichloromethane (2×300 mL). The combined organic layer was washed with water (2×200 mL), dried over anhydrous Mg2SO4 and filtered. The filtrate was evaporated under reduced pressure to afford 131b as a colorless oil (33.0 g, crude). 1H NMR (500 MHz, DMSO-d6) δ 9.99 (s, 1H), 2.62 (d, J=2.0 Hz, 2H), 2.38 (d, J=2.0 Hz, 2H), 1.15 (s, 6H).

후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureat reflux for 20 h
  3. temperatureThe reaction mixture was cooled to room temperature
  4. extractionThe mixture was extracted with dichloromethane (2×300 mL)
  5. washThe combined organic layer was washed with water (2×200 mL)
  6. dry with materialdried over anhydrous Mg2SO4
  7. filtrationfiltered
  8. customThe filtrate was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-cd3abb623e0f414fb562d45f4bcf2778
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115152B2

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