HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Benzyl-5-ethoxycarbonylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl 3-nitro-4-phenylacetylaminobenzoate | HCID 54219833 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Benzyl-5-ethoxycarbonylbenzimidazole | HCID 10221333 | 74.8% |
Reaction Steps
A mixture of 3.60 g of ethyl 3-nitro-4-phenylacetylaminobenzoate, 47 ml of ethanol, 23 ml of acetic acid and 6.4 g of reduced iron was heat-refluxed for 4 hours. The solid material was separated through filtration, and the filtrate was concentrated. To the residue were added 50 ml of ethanol and 5 g of 35% hydrochloric acid. The mixture was stirred for 40 hours while being heat-refluxed. The reaction solution was neutralized with sodium hydrogencarbonate, and was extracted with chloroform. The organic layer was concentrated under reduced pressure, and was purified through silica-gel column chromatography to give 2.30 g of 2-benzyl-5-ethoxycarbonylbenzimidazole (150).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352985B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-32210102b51748b088c707e3108cc102 |
| Source note | uspto-grants-2002_03 |