HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → 3,3'-[(3-Aminopropyl)azanediyl]di(propane-1,2-diol)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | 3,3'-Iminobispropane-1,2-diol | HCID 18403554 | — |
| Product | 3,3'-[(3-Aminopropyl)azanediyl]di(propane-1,2-diol) | HCID 23467798 | — |
Reaction Steps
Bis-(2,3-dihydroxypropyl)amine (16.5 g., 0.1 mole) and acrylonitrile (6.4 g., 0.12 mole) was mixed in an ice bath and then warmed to room temperature. After standing for 2 hours, the mixture was then heated at 45° C.-55° C. for 3 hours. The excess acrylonitrile was removed by gentle warming under reduced pressure. The residue was taken up in ethyl alcohol, mixed with sponge nickel catalyst and hydrogenated under 200 psi hydrogen using good agitation. After filtration of catalyst the solvent and excess acrylonitrile was removed by stripping under reduced pressure to leave the product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04065497 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-28d32870edd2402381fa8ed4a9f87658 |
| Source note | uspto-grants-1977_12 |