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Trifluoromethanesulfonic acid → 5-(Trifluoromethoxy)-2,3-dihydro-1H-inden-1-one

HRID 2060069
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반응식

HRID 2060069 반응식
FC(F)(F)S(O)(=O)=O.[F:9][C:10]([F:24])([F:23])[O:11][C:12]1[CH:13]=[C:14]([CH2:18][CH2:19][C:20]([OH:22])=O)[CH:15]=[CH:16][CH:17]=1>>[F:23][C:10]([F:9])([F:24])[O:11][C:12]1[CH:13]=[C:14]2[C:15](=[CH:16][CH:17]=1)[C:20](=[O:22])[CH2:19][CH2:18]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 62406Trifluoromethanesulfonic acidHCID 27772883-[3-(Trifluoromethoxy)phenyl]propanoic acid

생성물 1

HCID 221190265-(Trifluoromethoxy)-2,3-dihydro-1H-inden-1-one

실험 절차

About 37 ml of trifluoromethanesulfonic acid were added at about 5° C., with stirring, to 12.4 g of the product from step 1, and stirring was then carried out for 18 hours at room temperature. Crushed ice was then added, followed by extraction with diethyl ether. The combined organic phases were washed with saturated sodium hydrogen carbonate solution, water and saturated sodium chloride solution, and dried over magnesium sulfate, filtered and concentrated in vacuo at from 25 to 40° C. (yield 10.1 g).

후처리

  1. additionCrushed ice was then added
  2. extractionfollowed by extraction with diethyl ether
  3. washThe combined organic phases were washed with saturated sodium hydrogen carbonate solution, water and saturated sodium chloride solution
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • dry with materialdried over magnesium sulfate
  • filtrationfiltered
  • concentrationconcentrated in vacuo at from 25 to 40° C. (yield 10.1 g)
  • 출처 및 근거

    ORD 기록
    ord-630a782a7b454b4a88c2cf8d6053af96
    출처 데이터셋
    uspto-grants-2012_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08278338B2

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