HuagongsheHuagongshe Chemistry Print Report · For research reference only
Valeronitrile → HCID 178446835, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Valeronitrile | HCID 8061 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Morpholinoaniline hydrochloride | HCID 18952284 | — |
| Product | HCID 178446835 | HCID 178446835 | — |
Reaction Steps
A mixture of 4-(2-aminophenyl)morpholine hydrochloride (6.5 g) and valeronitrile (35 ml) were heated at 160°-165° C. under nitrogen for 25 hours and then cooled. The mixture was treated with aqueous sodium hydroxide and the basified mixture was extracted with dichloromethane. The solvent was removed by evaporation and the residue distilled under a pressure of 50 mm Hg to remove half the unreacted valeronitrile. A solid separated on cooling which was separated by filtration, washed with hexane (50 ml) and recrystallised from hexane to give N-(2-morpholinophenyl)valeramidine. (m.p. 135°-136° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05223498 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-b3b44186c5f44f568033d91384857498 |
| Source note | uspto-grants-1993_06 |