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Potassium Carbonate → 2-(3,3,4,4,4-Pentafluoro-butane-1-sulfonyl)-4-trifluoromethylsulfanyl-butyronitrile

HRID 80403
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HRID 80403 반응식
[F:1][C:2]([F:15])([C:11]([F:14])([F:13])[F:12])[CH2:3][CH2:4][S:5]([CH2:8][C:9]#[N:10])(=[O:7])=[O:6].[F:16][C:17]([S:20][CH2:21][CH2:22]OS(C(F)(F)F)(=O)=O)([F:19])[F:18].C([O-])([O-])=O.[K+].[K+]>COCCOC.O>[F:15][C:2]([F:1])([C:11]([F:12])([F:13])[F:14])[CH2:3][CH2:4][S:5]([CH:8]([CH2:22][CH2:21][S:20][C:17]([F:19])([F:18])[F:16])[C:9]#[N:10])(=[O:6])=[O:7]
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참가 물질

6

반응물 3

HCID 11430Potassium CarbonateHCID 252420282-(Trifluoromethylthio)ethyl TrifluoromethanesulfonateHCID 57425691(3,3,4,4,4-Pentafluorobutylsulfonyl)acetonitrile

생성물 1

HCID 529507362-(3,3,4,4,4-Pentafluoro-butane-1-sulfonyl)-4-trifluoromethylsulfanyl-butyronitrile

시약·촉매·용매 2

HCID 962Water용매
HCID 8071
1,2-Dimethoxyethane
용매

실험 절차

A mixture of (3,3,4,4,4-Pentafluoro-butane-1-sulfonyl)-acetonitrile (WO2007/060839) (0.50 g, 1.99 mmol), trifluoro-methanesulfonic acid 2-trifluoromethylsulfanyl-ethyl ester (WO 2007/147888) (0.55 g, 1.99 mmol), and K2CO3 (0.82 g, 5.97 mmol) in 1,2-dimethoxyethane (20 mL) was stirred under nitrogen at room temperature overnight. The reaction mixture was diluted with H2O (50 mL) and extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine (100 mL), dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (SiO2, hexanes/EtOAc 19:1) to afford compound II-1 (0.28 g, 37%) as a white solid.

후처리

  1. extractionextracted with ethyl acetate (2×50 mL)
  2. washThe combined organic extracts were washed with brine (100 mL)
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by column chromatography (SiO2, hexanes/EtOAc 19:1)
  6. customto afford compound II-1 (0.28 g, 37%) as a white solid

출처 및 근거

ORD 기록
ord-1bf14432504f4839beb54d5528a54b3b
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846569B2

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