HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576289Generated: November 3, 2026
Toluene → 1-(1,3-Dimethylureido)-3-(methylthio)propylphosphonic acid
https://huagongshe.com/reaction/1576289
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | N,N'-Dimethylurea | HCID 7293 | — |
| Reactant | Triphenyl phosphite | HCID 7540 | — |
| Reactant | Butanthial | HCID 12463483 | — |
| Product | 1-(1,3-Dimethylureido)-3-(methylthio)propylphosphonic acid | HCID 21501244 | — |
Reaction Steps
When a mixture of 0.5 mole each of 1,3-dimethylurea, triphenyl phosphite, and 3-methylthiopropionaldehyde in 100g of toluene is warmed to 75°, a reaction is initiated and the temperature increases rapidly to 120°. After further warming at 105° for 1 hr, the resulting yellow solution has a 31P nmr signal only at -28.2 ppm. After the solvent and most of the byproduct phenol are removed by stripping to 110°/1mm, one-third of the residue is dissolved in 75ml of acetonitrile and 10g of water, and this solution is refluxed for 3 hr. The reaction mixture is allowed to evaporate to dryness, and the residue is extracted with ether and then with hot acetonitrile and recrystallized twice from acetic acid to give a white solid: mp 164.5°-167°; 31P nmr (DMSO-d6) -21.4 ppm; 1H nmr δ9.6 (broad, 2, OH), 4.5 (m, 1, PCH), 2.8 (s, NCH3), 2.6 (s, NCH3), 2.0 (s, SCH3), 1.9-2.6 (m, CH2CH2S).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03980618 |
|---|
| Source dataset | uspto-grants-1976_09 |
|---|
| ORD ID | ord-69adae23bb3a4cf08751a9fd6a660665 |
|---|
| Source note | uspto-grants-1976_09 |
|---|