Reaction #550813

ord-0951276e791a46f08112c8d5d0d2ff55

Solvents

Conditions

Temperature
4°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Filtrationfiltered
  2. 2
    Concentrationconcentrated on a rotary evaporator at room temperature
  3. 3
    workup.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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04544501uspto-grants-1985_10