O-Phenylenediamine → Thiabendazole

HRID 1033528

反応式

HRID 1033528 の反応式
[C:1]1([NH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH2:7].[C:9]([C:11]1[N:12]=[CH:13][S:14][CH:15]=1)#N>O>[CH:4]1[CH:5]=[CH:6][C:1]2[N:8]=[C:9]([C:11]3[N:12]=[CH:13][S:14][CH:15]=3)[NH:7][C:2]=2[CH:3]=1

参加物

4

反応物 2

HCID 7243O-PhenylenediamineHCID 150694-Cyanothiazole

生成物 1

HCID 5430Thiabendazole収率 89.3%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
50 °C

実験手順

The product, thiabendazole, precipitated as it was formed in the reaction mixture. The reaction was monitored by gas chromatography and determined to be complete when the peaks corresponding to o-phenylenediamine and 4-cyanothiazole were negligible. The reaction mass was allowed to cool to 50° C. and 150 ml of 50° C. deionized water was added to thin the mixture before being vacuum filtered using a medium fritted glass filter. The solid product was washed four times with 300 ml portions of deionized water. The washed precipitate was dried overnight in a vacuum oven under 15-20" Hg and at a temperature of 80°-90° C. A total of 89.77 grams of thiabendazole were obtained which corresponds to an 89.3% yield. The color of dry thiabendazole was cream. High Performance Liquid Chromatography (HPLC) using a Hewlett-Packard Model 1090M showed that the purity was 98.77% (based on % area).

後処理

  1. customThe product, thiabendazole, precipitated as it
  2. customwas formed in the reaction mixture
  3. custom150 ml of 50° C.
  4. additionwas added
  5. filtrationfiltered
  6. filtrationfilter
  7. washThe solid product was washed four times with 300 ml portions of deionized water
  8. customThe washed precipitate was dried overnight in a vacuum oven under 15-20" Hg and at a temperature of 80°-90° C

出典と根拠

ORDレコード
ord-1942a8dab9ce4763b2b90060eddba93b
出典データセット
uspto-grants-1994_05
特許番号
US05310924

関連ノート

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