HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Ethyl 3-amino-l-(4-chlorophenyl)propyl(diethoxymethyl)phosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl 1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinate | HCID 14362807 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-amino-l-(4-chlorophenyl)propyl(diethoxymethyl)phosphinate | HCID 14362810 | — |
Reaction Steps
A solution of 20 g of ethyl 1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinate in 85 ml of ethanol is added to 131 g of an 8% solution of ammonia in ethanol. To this are added 8.5 ml of Raney Nickel and the resulting mixture is hydrogenated at 1 bar until the theoretical amount of hydrogen has been taken up. The mixture is then filtered, the filtrate is concentrated under reduced pressure and the crude product is distilled under reduced pressure to give ethyl 3-amino-1-(4-chlorophenyl)propyl(diethoxymethyl)phosphinate, b.p. 190° C./0.02 mbar, 31P=+41.5 and +41.3 ppm (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04656298 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-9b71f176d54d4d62975e52495602d2de |
| Source note | uspto-grants-1987_04 |