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3-Chloro-4-(trifluoromethyl)benzyl alcohol → 3-Chloro-4-(trifluoromethyl)benzaldehyde

HRID 1806839
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인쇄 미리보기

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HRID 1806839 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[C:10]([F:13])([F:12])[F:11])[CH2:5][OH:6]>ClCCCl.O=[Mn]=O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[C:10]([F:11])([F:12])[F:13])[CH:5]=[O:6]
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참가 물질

4

반응물 1

HCID 445579373-Chloro-4-(trifluoromethyl)benzyl alcohol

생성물 1

HCID 190312873-Chloro-4-(trifluoromethyl)benzaldehyde수율 60%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 111,2-Dichloroethane용매

반응 조건

온도
80 °C

실험 절차

Step A A mixture of 3-chloro-4-(trifluoromethyl)benzyl alcohol (Synquest) (4.77 g, 23 mmol) and activated MnO2 (19.5 g, 230 mmol) in 1,2-dichlorethane (80 mL) was heated and stirred at 80° C. for 3 h. The mixture was cooled to room temperature and filtered through a short pad of celite. The celite was washed with dichloromethane, and ethyl acetate. The filtrates were combined, concentrated, dried under reduced pressure to give 3-chloro-4-(trifluoromethyl)benzaldehyde as a light yellow oil (2.8 g, 60%).

후처리

  1. temperaturewas heated
  2. temperatureThe mixture was cooled to room temperature
  3. filtrationfiltered through a short pad of celite
  4. washThe celite was washed with dichloromethane, and ethyl acetate
  5. concentrationconcentrated
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-86b6bde40e0747a296759688ef21f51e
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354444B2

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