HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 2-methoxyphenyl ketone → 2-Amino-1-benzylideneamino-4-(2-methoxyphenyl)-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 2-methoxyphenyl ketone | HCID 123440 | — |
| Reactant | HCID 178513139 | HCID 178513139 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-1-benzylideneamino-4-(2-methoxyphenyl)-imidazole | HCID 54145412 | — |
Reaction Steps
A solution of 41.7 g (0.257 mol) of benzaldehyde guanylhydrazone (see Thiele, A., Liebigs Annalen der Chemie 270, 35) and 30.12 g of 2-methoxyphenacyl bromide (Aldrich, Buchs, Switzerland; 98%, Cat. no. 10,085-4) in 130 ml of ethanol is boiled under reflux for one hour. After cooling, the product that has crystallised out is filtered off with suction and recrystallized from ethanol. In that manner there is obtained the title compound, m.p. 166°-167° C., 1H-NMR (DMSO): δ=8.61 (s, 1H); 8.0 (m, 3H); 7.88 (s, 1H); 7.5 (m, 3H); 7.19 (m, 1H); 7.03 (d, 1H); 6.96 (t, 1H); 6.16 (s, 2H); 3.94 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840911 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-2f68083a6a144c5c80812bf0a9653c0c |
| Source note | uspto-grants-1998_11 |