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Cyclopropyl methyl ketone → (NE)-N-(1-cyclopropylethylidene)-2-methylpropane-2-sulfinamide

HRID 246611
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HRID 246611 반응식
[CH:1]1([C:4](=O)[CH3:5])[CH2:3][CH2:2]1.[CH3:7][C:8]([S:11]([NH2:13])=[O:12])([CH3:10])[CH3:9]>C1COCC1>[CH:1]1(/[C:4](=[N:13]/[S:11]([C:8]([CH3:10])([CH3:9])[CH3:7])=[O:12])/[CH3:5])[CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 13004Cyclopropyl methyl ketoneHCID 3382465Tert-Butanesulfinamide

생성물 1

HCID 89421056(NE)-N-(1-cyclopropylethylidene)-2-methylpropane-2-sulfinamide수율 27%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 1-cyclopropylethanone (1 g, 12 mmol), 2-methylpropane-2-sulfinamide (1.7 g, 14 mmol), Ti(OEt)4 (5.5 g, 24 mmol) in 10 mL of THF was heated at reflux with stirring overnight. The mixture was cooled to room temperature, solvent was removed under reduced pressure and the crude residue was purified by column chromatography (silica gel, 200-300 mesh, petroleum ether and ethyl acetate (3:1, v/v) to give (E)-N-(1-cyclopropylethylidene)-2-methylpropane-2-sulfinamide (0.6 g, 27%) as clear oil. MS: (M+H)+=188.2; 1H NMR (300 MHz, CDCl3): δ 2.36 (s, 3H), 1.69 (m, 1H), 1.18 (s, 9H), 1.07-0.89 (m, 4H).

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후처리

  1. temperaturewas heated
  2. temperatureat reflux
  3. customsolvent was removed under reduced pressure
  4. customthe crude residue was purified by column chromatography (silica gel, 200-300 mesh, petroleum ether and ethyl acetate (3:1

출처 및 근거

ORD 기록
ord-6f96dc3d5ef041cd9850b2d5db0c244c
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658646B2

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