Sulfuric Acid → N-tert-butylpyrazine-2-carboxamide

HRID 582246

반응식

HRID 582246 반응식
S(=O)(=O)(O)O.[C:6]([C:8]1[CH:13]=[N:12][CH:11]=[CH:10][N:9]=1)#[N:7].[C:14](O)([CH3:17])([CH3:16])[CH3:15].[OH-:19].[Na+]>O>[C:14]([NH:7][C:6]([C:8]1[CH:13]=[N:12][CH:11]=[CH:10][N:9]=1)=[O:19])([CH3:17])([CH3:16])[CH3:15]

참가 물질

6

반응물 4

HCID 1118Sulfuric AcidHCID 6386tert-ButanolHCID 14798Sodium HydroxideHCID 73172Pyrazinecarbonitrile

생성물 1

HCID 4462842N-tert-butylpyrazine-2-carboxamide

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To 1030 g of an 80% aqueous solution of sulfuric acid (8.40 moles of sulfuric acid), 220.5 g (2.1.0 moles) of 2-cyanopyrazine was added dropwise keeping the internal temperature at 40° C. or less with stirring. In succession, 187 g (2.52 moles) of tert-butyl alcohol was added dropwise to the mixture of which internal temperature was kept at 9° to 15° C. over 3 hours. Further, the temperature was kept at the same temperature for 2.5 hours. After that, the reaction liquid was poured into 3500 g of water with stirring. Thus obtained mixture was neutralized with an aqueous solution of sodium hydroxide. The precipitated crystalline solid was separated by filtration, washed with water and dried to obtain 338.7 g (1.89 moles) of N-tert-butyl-2-pyrazinecarboxamide. It had a melting point of 88° to 90° C. Further, from the filtrate 7.17 g (0.04 mole) of N-tert-butyl-2-pyrazine-carboxamide was further obtained by extraction thereof with toluene. The yield thereof was 91.9%.

후처리

  1. customat 40° C. or less
  2. waitFurther, the temperature was kept at the same temperature for 2.5 hours
  3. customAfter that, the reaction liquid
  4. stirringwith stirring
  5. customThe precipitated crystalline solid was separated by filtration
  6. washwashed with water
  7. customdried

출처 및 근거

ORD 기록
ord-67bfbf4fc3fa46f5a3ac06040410d88e
출처 데이터셋
uspto-grants-1999_07
특허 번호
US05922873

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