HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → Butyl ethyl(2-cyanoethyl)phosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Sodium n-butylate | HCID 23669364 | — |
| Reactant | Butyl ethyiphosphonite | HCID 86614949 | — |
| Product | Butyl ethyl(2-cyanoethyl)phosphinate | HCID 19606949 | 90% |
Reaction Steps
A 1 l five-neck flask equipped with thermometer, reflux condenser, high-performance stirrer and dropping funnel was initially charged with 447 g (3 mol) of butyl ethylphosphonite (produced as in Example 2) and 159 g (3 mol) of acrylonitrile. While stirring, 15 ml of sodium butoxide (30% strength in butanol) are added dropwise at such a rate that a reaction temperature of max. 120° C. becomes established. The crude product thus obtained is distilled in vacuo to obtain 548 g (90% of theory) of butyl ethyl(2-cyanoethyl)phosphinate as colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09035088B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-4617faedb40d4a5fa98f10c540e51397 |
| Source note | uspto-grants-2015_05 |