Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 54098565 | HCID 54098565 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19836622 | HCID 19836622 | 65% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04544501 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-0951276e791a46f08112c8d5d0d2ff55 |
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| Source note | uspto-grants-1985_10 |
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