HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 86741818, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 178525532 | HCID 178525532 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 86741818 | HCID 86741818 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04696763 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-da25f27ad3fa434abba9e6bf5f683b58 |
| Source note | uspto-grants-1987_09 |