Water → 2-Methylbenzo(d)thiazole-5-carbonitrile

HRID 53954

反応式

HRID 53954 の反応式
Br[C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]([CH3:10])=[N:7][C:6]=2[CH:11]=1.O.[CH3:13][N:14]1CCCC1=O>S([O-])([O-])(=O)=O.[Cu+2]>[CH3:10][C:8]1[S:9][C:5]2[CH:4]=[CH:3][C:2]([C:13]#[N:14])=[CH:11][C:6]=2[N:7]=1

参加物

5

実験手順

28.0 g of 5-bromo-2-methylbenzothiazole was dissolved in 200 ml of N-methyl-2-pyrrolidone, the solution thus prepared was mixed with 13.8 g of cuprous cyanide and a catalytically effective amount of copper sulfate, and the mixture was stirred for 4 hours with heating at a temperature of 180° to 190° C. in a stream of nitrogen. The resulting reaction solution was poured into water, and insoluble materials thus formed were collected by filtration. The thus collected insoluble materials were mixed with a mixture consisting of 22 ml of methylenediamine and 50 ml of water, and the resulting mixture was stirred thoroughly. After extraction with benzene, the resulting organic layer was washed with water, and dried to distill of benzene. Thereafter, the residue thus formed was washed with ethanol to obtain 10.22 g of 2-methyl-5-benzothiazolecarbonitrile in the form of light brown crystals.

後処理

  1. customthe solution thus prepared
  2. temperaturewith heating at a temperature of 180° to 190° C. in a stream of nitrogen
  3. customThe resulting reaction solution
  4. customthus formed
  5. filtrationwere collected by filtration
  6. additionThe thus collected insoluble materials were mixed with a mixture
  7. extractionAfter extraction with benzene
  8. washthe resulting organic layer was washed with water
  9. customdried
  10. distillationto distill of benzene
  11. customThereafter, the residue thus formed
  12. washwas washed with ethanol

出典と根拠

ORDレコード
ord-f678b99062454396a387fe80d8b5cdb1
出典データセット
uspto-grants-1997_04
特許番号
US05620991

関連ノート

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