HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diallylamine → ethyl N-trifluoroacetyl-N-(bis(diallylamino)phosphonomethyl)glycinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diallylamine | HCID 31279 | — |
| Reactant | Ethyl N-trifluoroacetyl-N-(dichlorophosphonomethyl)glycinate | HCID 23345669 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl N-trifluoroacetyl-N-(bis(diallylamino)phosphonomethyl)glycinate | HCID 53906450 | — |
Reaction Steps
To a solution of ethyl N-trifluoroacetyl-N-(dichlorophosphonomethyl)glycinate (3.3 g, 0.01 mole) in 25 ml. of tetrahydrofuran was added diallylamine (4.07 g, 0.042 mole) in 50 ml. of tetrahydrofuran. The mixture was stirred at room temperature overnight and was then filtered and the filtrate concentrated in vacuo. The residue was dissolved in ether, washed with water, 10% HCl, water, dried over MgSO4, and concentrated in vacuo. The residue was extracted with petroleum ether, and by concentrating the petroleum ether soluble material, ethyl N-trifluoroacetyl-N-(bis(diallylamino)phosphonomethyl)glycinate was obtained as a light yellow oil, ND =1.4536.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04353731 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-7fe57b65955b4769a432fd214fce4259 |
| Source note | uspto-grants-1982_10 |