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Sulfoxonium, trimethyl-, iodide (1:1) → HCID 57810032, 화합물

HRID 2106031
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HRID 2106031 반응식
[F:1][C:2]([F:22])([F:21])[C:3](=[O:20])[CH2:4][C:5]([CH3:19])([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([C:13]2([CH3:18])[O:17][CH2:16][CH2:15][O:14]2)[CH:8]=1)[CH3:6].[Na].[I-].[CH3:25][S+](C)(C)=O>CS(C)=O>[CH3:19][C:5]([C:7]1[CH:8]=[C:9]([C:13]2([CH3:18])[O:14][CH2:15][CH2:16][O:17]2)[CH:10]=[CH:11][CH:12]=1)([CH3:6])[CH2:4][C:3]1([C:2]([F:1])([F:21])[F:22])[CH2:25][O:20]1
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5

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HCID 74498Sulfoxonium, trimethyl-, iodide (1:1)HCID 5360545SodiumHCID 578100111,1,1-Trifluoro-4-methyl-4-[3-(2-methyl-[1,3]dioxolan-2-yl)phenyl]pentan-2-one

생성물 1

HCID 57810032HCID 57810032, 화합물

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매2회

실험 절차

To a solution of 1,1,1-trifluoro-4-methyl-4-[3-(2-methyl-[1,3]dioxolan-2-yl)phenyl]pentan-2-one (0.56 g, 1.8 mmol) in anhydrous DMSO (2.3 mL) was added the sodium ylide of trimethylsulfoxonium iodide (2.6 mL of a 0.8M solution in DMSO) over 5 minutes. The mixture was stirred 2 hours, quenched with water, and extracted with ethyl acetate. The combined organic layers were washed with water and brine, and dried over sodium sulfate. The solution was concentrated in vacuo to afford the yellow oil, 2-{3-[1,1-dimethyl-2-(2-trifluoromethyloxiranyl)ethyl]phenyl}-2-methyl-[1,3]dioxolane, which was used without further purification.

후처리

  1. customquenched with water
  2. extractionextracted with ethyl acetate
  3. washThe combined organic layers were washed with water and brine
  4. dry with materialdried over sodium sulfate
  5. concentrationThe solution was concentrated in vacuo

출처 및 근거

ORD 기록
ord-688ad17e84554d9385870f5ea7bbfb57
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07579469B2

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