HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → isobutyl P-(3-aminopropyl)-P-methyl-phosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | isobutyl P-(2-cyanoethyl)-P-methyl-phosphinate | HCID 2304642 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | isobutyl P-(3-aminopropyl)-P-methyl-phosphinate | HCID 23374769 | — |
Reaction Steps
A solution of 20.0 g of isobutyl P-(2-cyanoethyl)-P-methyl-phosphinate in 200 ml of ethanol is added to 230.0 g of an 8% solution of ammonia in ethanol. To this are added 15 ml of Raney nickel slurry and the resulting mixture is hydrogenated at 1 bar until hydrogen uptake ceases. The mixture is then filtered and the filtrate is concentrated under reduced pressure. The crude product is distilled under reduced pressure to give isobutyl P-(3-aminopropyl)-P-methyl-phosphinate, b.p. 130°/0.01 mbar, 31P-NMR spectrum: δ=+57.6 ppm (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05567840 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-f8750e33080e4bde9e83ffe79323d8c1 |
| Source note | uspto-grants-1996_10 |