HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 13098806, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 13098801 | HCID 13098801 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13098806 | HCID 13098806 | 20% |
Reaction Steps
A mixture of N-methyl-N-[3,4-(methylenedioxy)phenyl]urea (240 mg), benzaldehyde (140 μL) and methanesulfonic acid (50 μL) and toluene (60 mL) was refluxed for 2 h in a flask equipped with a Dean-Stark water separator. After cooling, the solution was washed with water thoroughly, dried over Na2SO4 and concentrated in vacuo. The resulting solid was recrystallized from chloroform/hexane to provided the title compound as a tan solid (70 mg, 20%), mp: 228-230° C. 1H NMR (CDCl3): 7.37-7.30 (m, 5H), 6.53 (s, 1H), 6.28 (s, 1H), 5.91 (d, 1H, J=1.4), 5.89 (d, 1H, J=1.4), 5.46 (s, 1H), 5.11 (br s, 1H), 3.33 (s, 3H). Anal. calcd. for C16H14N2O3: C, 68.08; H, 5.00; N, 9.92. Found: C, 68.06; H, 4.91; N, 9.71.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652006B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-4051016f9ab94513a545ab523cfa7e12 |
| Source note | uspto-grants-2010_01 |