HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476849Generated: October 27, 2026
N,N-Dimethyl-1,3-propanediamine → P,P-bis(2,2-dimethyl-1-aziridinyl)-N-(3-dimethylaminopropyl)phosphinic amide
https://huagongshe.com/reaction/476849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | P,P-bis(2,2-dimethyl-1-aziridinyl)phosphinyl chloride | HCID 13511140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | P,P-bis(2,2-dimethyl-1-aziridinyl)-N-(3-dimethylaminopropyl)phosphinic amide | HCID 366242 | 40% |
Reaction Steps
A solution containing 0.025 moles of P,P-bis(2,2-dimethyl-1-aziridinyl)phosphinyl chloride in about 170 milliliters of THF was prepared in accordance with Example 1, chilled to -40° C. and treated, by slow dropwise addition, with a solution containing 0.026 moles of 3-dimethylaminopropylamine, in 25 milliliters of THF. The resulting slurry was stirred overnight at ambient temperature, filtered, the filtrate was concentrated by rotary evaporation, and vacuum distilled at 119° C./0.45 millimeter of mercury to produce a 40% yield of P,P-bis(2,2-dimethyl-1-aziridinyl)-N-(3-dimethylaminopropyl)phosphinic amide. NMR characterization confirmed the product was 99% pure. Elemental analysis confirmed the structure contained the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04886790 |
|---|
| Source dataset | uspto-grants-1989_12 |
|---|
| ORD ID | ord-90a0f3d7742b47f7ac28741abd2a5edd |
|---|
| Source note | uspto-grants-1989_12 |
|---|