반응 #3744

ord-b0a5f477af2d4178b1eacf13ac36441b

반응 방정식

CC(C)(C)O
tert-butyl alcohol
O=S(=O)(O)O
sulfuric acid
N#Cc1cnccn1
2-cyanopyrazine
[Na+].[OH-]
sodium hydroxide
CC(C)(C)NC(=O)c1cnccn1
N-tert-butyl-2-pyrazinecarboxamide

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타at 40° C. or less
  2. 2
    workup.WAITFurther, the temperature was kept at the same temperature for 2.5 hours
  3. 3
    기타After that, the reaction liquid
  4. 4
    workup.STIRRINGwith stirring
  5. 5
    기타The precipitated crystalline solid was separated by filtration
  6. 6
    세척washed with water
  7. 7
    기타dried

실험 절차

To 1030 g of an 80% aqueous solution of sulfuric acid (8.40 moles of sulfuric acid), 220.5 g (2.10 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%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05734055uspto-grants-1998_03