HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → Butyl ethyl(3-aminopropyl)phosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Butyl ethyiphosphonite | HCID 86614949 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Butyl ethyl(3-aminopropyl)phosphinate | HCID 46212699 | 65.1% |
Reaction Steps
150 g (1 mol) of butyl ethylphosphonite (produced as in Example 2) and 68.4 g (1.2 mol) of allylamine are initially charged in 200 ml of butanol in a four-neck round-bottom flask equipped with stirrer, reflux condenser, thermometer and nitrogen inlet, and heated. At about 100° C., in the course of 1 h, 98.4 g of a 5% solution of AIBN in butanol are added dropwise, whereafter the solvent is distilled off in vacuo. Chromatographic purification yields 135 g (65% of theory) of butyl ethyl(3-aminopropyl)phosphinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604232B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-648ac24811eb4fe29028af2f65dc5e13 |
| Source note | uspto-grants-2013_12 |