HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N'-Dimethylurea → Phosphonium, tetrakis((methyl((methylamino)carbonyl)amino)methyl)-,chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N'-Dimethylurea | HCID 7293 | — |
| Reactant | Tetrakis(hydroxymethyl)phosphonium chloride | HCID 31298 | — |
| Product | Phosphonium, tetrakis((methyl((methylamino)carbonyl)amino)methyl)-,chloride | HCID 153314 | 25% |
Reaction Steps
A solution of 80% THPC (59.55 g, 0.25 mol) and 1,3-dimethylurea (88.12 g, 1 mol) was heated to reflux in an oil bath, held at reflux for 4 hrs., allowed to cool, and stripped to dryness in a rotary evaporator. The residue (130.67 g) was shaken with acetonitrile (100 ml) and filtered, giving 29.40 g (25.0%) of tetrakis(1,3-dimethylureidomethyl)phosphonium chloride (I, R=R'=CH3, R"=H, X=Cl) as a white, crystalline solid, mp 189°-190° C. dec. The remainder, a heavy oil, yielded no more product nor water even when subjected to azeotropic distillation with toluene and more 1,3-dimethylurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04265945 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-8e70f61cc33e4cb8996ffa64d4fd6311 |
| Source note | uspto-grants-1981_05 |