HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 1-isopropyl-4-phenyl-6,7-methylenedioxy-3,4-dihydro-2(1H)-quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Methane | HCID 297 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-(1,3-Benzodioxol-5-yl)-1-isopropylurea | HCID 100555 | — |
| Catalyst | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 1-isopropyl-4-phenyl-6,7-methylenedioxy-3,4-dihydro-2(1H)-quinazolinone | HCID 12789469 | — |
Reaction Steps
A solution of 10.3 gm. of N-isopropyl-(3,4-methylenedioxyphenyl)urea, 7.1 ml. of benzaldehyde, and 3 drops of methanesulphonic acid in 250 ml. of toluene is refluxed under a water separator for 21 hours. The cooled solution is then washed with 200 ml. of water, dried and evaporated to yield a powder. This product is decolorized in hot propanol with a small amount of activated charcoal and recrystallized from propanol to obtain 1-isopropyl-4-phenyl-6,7-methylenedioxy-3,4-dihydro-2(1H)-quinazolinone, m.p. 169°-172°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997564 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-8bd7f384ee8841eb8f343841c2fa2646 |
| Source note | uspto-grants-1976_12 |