HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N,N'-Dicyclohexylurea | HCID 4277 | — |
Reaction Steps
The copolymer was fed into a round-bottomed flask and dissolved in a half amount (25 to 30 mL) of ethyl acetate. Next, N-hydroxysuccinimide and DCC were added thereto followed by dissolution in the residual ethylacetate. The obtained mixture was immersed in ice-water at 4° C. and stirred with a stirrer for 2 hours. Subsequently, it was introduced into a thermostat at 25° C. and stirred therein overnight. The solution was filtered and thus dicyclohexyl urea formed as a by product was removed therefrom. After concentrating under reduced pressure, the residue was purified with diethyl ether. The product thus obtained was taken up by filtration and dried under reduced pressure. The succinylated copolymer thus obtained was stored in a freezer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706187B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-04f9ce3b4a994751845b4f99bd59f232 |
| Source note | uspto-grants-2004_03 |