Reaction #550813
ord-0951276e791a46f08112c8d5d0d2ff55
Reaction equation
Reagents
None
Solvents
Conditions
Temperature
4°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1Filtrationfiltered
- 2Concentrationconcentrated on a rotary evaporator at room temperature
- 3workup.DISTILLATIONvacuum distilled
Procedure
In a similar manner 0.025 moles of P,P-bis(2,2-dimethyl-1-aziridinyl)thiophosphinic bromide in about 170 milliliters of THF, prepared in accordance with Example 1, is saturated with an excess of gaseous methylamine, stirred over night at 4° C., filtered, concentrated on a rotary evaporator at room temperature, and vacuum distilled to provide about 65% yield of P,P-bis(2,2-dimethyl-1-aziridinyl)-N methylthiophosphinic amide.