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Dicyclohexylcarbodiimide → Benzothiazol-2-ylthio succinic anhydride

HRID 2309670
ノート
印刷プレビュー

反応式

HRID 2309670 の反応式
C1(N=C=NC2CCCCC2)CCCCC1.[S:16]1[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[N:18]=[C:17]1[CH:25]([CH2:29][C:30]([OH:32])=[O:31])[C:26](O)=[S:27]>C(COC)OC>[S:16]1[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[N:18]=[C:17]1[CH:25]1[CH2:29][C:30](=[O:31])[O:32][C:26]1=[S:27]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10868DicyclohexylcarbodiimideHCID 178525532HCID 178525532、化合物

生成物 1

HCID 86741818Benzothiazol-2-ylthio succinic anhydride

試薬・触媒・溶媒 1

HCID 80711,2-Dimethoxyethane溶媒2 回

実験手順

A solution of 6.18 parts of dicyclohexylcarbodiimide in 30 parts by volume of dimethoxyethane is added dropwise, over 1.5 hours, to a stirred solution of 8.49 parts of benzothiazol-2-ylthio succinic acid prepared as in Example 1A in dimethoxyethane (70 parts by volume). The reaction is exothermic and the temperature is maintained at 25°-27° with cooling. When the addition is complete, stirring is continued for a further 1.5 hours and the precipitated dicyclohexylurea is removed by filtration. The filtrate is evaporated in vacuo and the residual solid is recrystallised from a mixture of dichloromethane and cyclohexane to give benzothiazol-2-ylthio succinic anhydride m.p. 129°-129° (with decomposition).

後処理

  1. temperaturethe temperature is maintained at 25°-27°
  2. temperaturewith cooling
  3. additionWhen the addition
  4. customthe precipitated dicyclohexylurea is removed by filtration
  5. customThe filtrate is evaporated in vacuo
  6. customthe residual solid is recrystallised from a mixture of dichloromethane and cyclohexane

出典と根拠

ORDレコード
ord-da25f27ad3fa434abba9e6bf5f683b58
出典データセット
uspto-grants-1987_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04696763

反応ノート

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