HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → N-(1-Methyldecyl)-3-phenyl-3-(4-nitrophenyl)propenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-Undecanamine | HCID 114476 | — |
| Reactant | 3-(4-Nitrophenyl)-3-phenylprop-2-enoic acid | HCID 53427600 | — |
| Product | N-(1-Methyldecyl)-3-phenyl-3-(4-nitrophenyl)propenamide | HCID 53836625 | 51% |
Reaction Steps
The title compound was prepared from 3-phenyl-3-(4-nitrophenyl)propenoic acid via mixed anhydride formation using ethyl chloroformate, followed by reaction with 1-methyldecylamine, substantially according to the procedure of Preparation 21. The product was induced to solidify by trituration under hexane. The solid was recrystallized from hexane, giving a small amount of material which was discarded. The mother liquors were evaporated in vacuo to give an oil which solidified when stirred under acetonitrile. The solid was filtered off, giving a 51% yield of the title compound, m.p. 69°-71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04342781 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-ca363b7f65534cd6b1c78e535ccde923 |
| Source note | uspto-grants-1982_08 |