HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → P,P-bis(2,2-dimethyl-1-aziridinyl)-N,N-dimethylthiophosphinic amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorothioic tribromide | HCID 77530 | — |
| Reactant | 2,2-Dimethylaziridine | HCID 227244 | — |
| Product | P,P-bis(2,2-dimethyl-1-aziridinyl)-N,N-dimethylthiophosphinic amide | HCID 19836619 | 65% |
Reaction Steps
In a similar manner 0.16 moles of triethylamine, 0.05 moles of PSBr3 and 150 milliliters of dried tetrahydrofuran are combined in a 250 milliliter round bottom flask which is thereafter treated with a first solution containing 0.10 moles of 2,2-dimethylaziridine in 20 milliliters of THF and a second solution containing 0.16 moles of dimethylamine in 25 millimeters of dried THF, to produce a slurry which after filtration, concentration of the filtrate and vacuum distillation affords about 65% yield of P,P-bis(2,2-dimethyl-1-aziridinyl)-N,N-dimethylthiophosphinic amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04544501 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-decd575cb21e4d9594997b1490b87d86 |
| Source note | uspto-grants-1985_10 |