HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 21536081, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Methylurea | HCID 11719 | — |
| Reactant | 1,3-Bis(3-chlorophenyl)propane-1,3-dione | HCID 226782 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21536081 | HCID 21536081 | — |
Reaction Steps
To a solution of 38 g. di(m-chlorobenzoyl)methane in 400 ml. glacial acetic acid is added 23 g. N-methylurea and 57 g. p-toluene sulfonic acid. This mixture is refluxed for 24 hours and acetic acid removed by evaporation in vacuo. The residue is treated with 2N. sodium hydroxide till basic, extracted several times with methylene chloride. The combined methylene chloride extracts are then exhaustively extracted with water, dried and evaporated in vacuo to dryness. The residue is crystallized from methylene chloride/diethyl ether and then twice from benzene to obtain 1-methyl-4,6-di(m-chlorophenyl)-pyrimidine-2(1H)-one, m.p. 178°-181°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959471 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-acea7b078cc24d8788e3900335e59a3a |
| Source note | uspto-grants-1976_05 |