HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 3-methoxyphenyl ketone → 2-Amino-1-benzylideneamino-4-(3-methoxyphenyl)-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 3-methoxyphenyl ketone | HCID 101294 | — |
| Reactant | HCID 178513139 | HCID 178513139 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-1-benzylideneamino-4-(3-methoxyphenyl)-imidazole | HCID 54047753 | — |
Reaction Steps
A solution of 16.2 g (0.1 mol) of benzaldehyde guanylhydrazone and 11.8 g (0.050 mol) of 3-methoxyphenacyl bromide (Aldrich, Buchs, Switzerland; 98 %, Cat. no. 11,567-3) in 50 ml of ethanol is stirred at 20° C. for 3 hours. The product that has crystallized out is filtered off with suction and dried. In that manner there is obtained the title compound, m.p. 170°-171° C., 1H-NMR (DMSO): δ=8.56 (s, 1H); 8.03 (s, 1H); 7.92 (m, 2H); 7.5 (m, 3H); 7.26 (m, 3H); 6.76 (m, 1H); 6.2 (s, 2H); 3.8 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840911 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-a4af0387c5784795ac984847918570e8 |
| Source note | uspto-grants-1998_11 |