HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthopropionate → HCID 21254783, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthopropionate | HCID 66995 | — |
| Reactant | HCID 21254704 | HCID 21254704 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21254783 | HCID 21254783 | 67.7% |
Reaction Steps
To a stirred solution of 2-amino-3-(4-methoxybenzyloxy)-aniline (1.15 g) in acetic acid (12 ml) was added triethyl orthopropionate (994 mg) at ambient temperature, and the mixture was stirred overnight. The reaction mixture was concentrated in vacuo, and the residue was extracted with dichloromethane. The organic layer was washed with saturated sodium bicarbonate solution and brine, dried over magnesium sulfate and evaporated in vacuo to give 2-ethyl-4-(4-methoxybenzyloxy)-1H-benzimidazole (900 mg) as pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194396B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-b05f6d0de7514da9a35e5c81465f1785 |
| Source note | uspto-grants-2001_02 |