HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthoformate → ethyl 3-benzyl-3H-benzo[d]imidazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Ethyl 4-amino-3-(benzylamino)benzoate | HCID 58213838 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 3-benzyl-3H-benzo[d]imidazole-5-carboxylate | HCID 58213808 | 48.1% |
Reaction Steps
A solution of ethyl 4-amino-3-(benzylamino)benzoate (0.24 g, 0.89 mmol) and triethyl orthoformate (0.8 mL, 4.8 mmol) in ethanol (10 mL) and conc. HCl (7 drops) was heated to reflux for 24 hr. The solution was cooled to room temperature and concentrated, then diluted with ethyl acetate (100 mL) and washed with dilute aq. NaHCO3 (1×100 mL). Then organic layer was dried (MgSO4), filtered and then concentrated and the resulting residue was purified by flash chromatography (50% ethyl acetate/hexane then ethyl acetate) to provide 0.12 g (48%) of ethyl 3-benzyl-3H-benzo[d]imidazole-5-carboxylate as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08906954B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-4246395bea3945119a2cfce70560035f |
| Source note | uspto-grants-2014_12 |