Water → N,N'-dimethoxy-N,N'-dimethylbutanediamide

HRID 490799

반응식

HRID 490799 반응식
[C:1](Cl)(=[O:7])[CH2:2][CH2:3][C:4](Cl)=[O:5].Cl.[CH3:10][NH:11][O:12][CH3:13].[N:14]1C=CC=C[CH:15]=1.[OH2:20].Cl[CH2:22]Cl>>[CH3:22][O:20][N:14]([CH3:15])[C:1](=[O:7])[CH2:2][CH2:3][C:4]([N:11]([O:12][CH3:13])[CH3:10])=[O:5]

참가 물질

6

실험 절차

Dissolve 136.2 g of succinyl dichloride and 180.0 g N,O-dimethylhydroxylamine hydrochloride in 1.2 L dichloromethane and cool it in an ice bath. Add 305.9 g pyridine from an addition funnel with stir over 1.5 hours. Let the reaction mixture warm up to room temperature over night. Pour the reaction mixture into ice and water and separate the layers. Wash the organic layer with cold 2 N HCl (2×), water, 5% NaHCO3 (2×), and saturated brine. Dry over anhydrous Na2SO4 and evaporate to give crude product. It was washed with 3:1 hexanes and dichloromethane and dried to give the title compound as a light tan solid 1H NMR (CDCl3, 500 MHz δ: 3.70 (s, 6H), 3.15 (s, 6H), 2.74 (s, 4H).

후처리

  1. temperaturecool it in an ice bath
  2. customseparate the layers
  3. washWash the organic layer with cold 2 N HCl (2×), water, 5% NaHCO3 (2×), and saturated brine
  4. dry with materialDry over anhydrous Na2SO4
  5. customevaporate
  6. customto give crude product
  7. washIt was washed with 3:1 hexanes and dichloromethane
  8. customdried

출처 및 근거

ORD 기록
ord-7fe6b6bc418f4397a56f52d339a64eeb
출처 데이터셋
uspto-grants-2009_05
특허 번호
US07528163B2

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