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Acetaldehyde → (E)-N-ethylidene-2-methylpropane-2-sulfinamide

HRID 1058263
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HRID 1058263 반응식
[CH3:1][C:2]([S@@:5]([NH2:7])=[O:6])([CH3:4])[CH3:3].[CH:8](=O)[CH3:9]>ClCCl.[O-]S([O-])(=O)=O.[Cu+2]>[CH:8](=[N:7][S:5]([C:2]([CH3:4])([CH3:3])[CH3:1])=[O:6])[CH3:9]
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참가 물질

5

반응물 2

HCID 177AcetaldehydeHCID 11355477tert-Butylsulfinamide, (S)-(-)-

생성물 1

HCID 73164120(E)-N-ethylidene-2-methylpropane-2-sulfinamide

시약·촉매·용매 2

HCID 24462Copper Sulfate촉매HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of (S)-(−)-2-methyl-2-propanesulfinamide (1.0 g, 8.25 mmol) and acetaldehyde (2.0 mL, 35.61 mmol) in dichloromethane (20 mL) at ambient temperature under nitrogen atmosphere was added CuSO4 (2.9 g, 18.15 mmol). The mixture was stirred at ambient temperature for 18 h. The reaction was filtered through celite and the filtrate solvent was removed under reduced pressure. N-ethylidene-2-methyl-2-propanesulfinamide was obtained as a clear colorless oil (1.18 g; 1H NMR, 400 MHz, CDCl3, 8.8 ppm (q, 11H), 2.24 ppm (d, 3H), 1.2 ppm (s, 9H)).

후처리

  1. filtrationThe reaction was filtered through celite
  2. customthe filtrate solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-68baf1705349404e9244b2c0dde66ce0
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06515011B2

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