HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Sodium 4-hydroxy-3-nitrobenzenesulfonate | HCID 12598197 | — |
| Reactant | N-maleimido-6-aminocaproic acid | HCID 19361018 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N'-Dicyclohexylurea | HCID 4277 | — |
Reaction Steps
One molar equivalent (2.24 g) of 4-hydroxy-3-nitrobenzene sulfonic acid sodium salt (HNSA) was mixed together with one molar equivalent (2.06 g) of dicyclohexylcarbodiimide and one molar equivalent (2.10 g) of N-maleimido-6-aminocaproic acid in 25 ml of dimethylformamide (DMF) at room temperature overnight. A white precipitate of dicyclohexyl urea was formed. The precipitate was filtered and 300 ml diethyl ether was added to the mother liquor. After about 10 minutes to 4 hours a gummy solid precipitated from the mother liquor was formed. This solid was found to contain 58% of active HNSA ester and 42% of free HNSA.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04762706 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-717c3c9f06e542e881321a78bdb17815 |
| Source note | uspto-grants-1988_08 |