HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → 3-[1-(4-Nitrobenzyl)benzimidazol-2-yl]-2-(carboethoxy)propanoic acid, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2,2-Diethylpropanedioate | HCID 6951563 | — |
| Reactant | HCID 14722476 | HCID 14722476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-[1-(4-Nitrobenzyl)benzimidazol-2-yl]-2-(carboethoxy)propanoic acid, ethyl ester | HCID 14722477 | — |
Reaction Steps
The sodium salt of diethylmalonate was generated from 0.35 g of NaH (50% oil dispersion) and 1.1 mL of diethyl malonate in 15 mL of dried DMF with ice cooling. To the above mixture was added 2 g of 1-(4-nitrobenzyl)-2-chloromethylbenzimidazole and the mixture was stirred at room temperature for 18 hours. The reaction mixture was diluted with ethyl acetate, washed with water, dried and concentrated in vacuo. The crude produce was purified by flash column chromatography (hexane/ethyl acetate, 1:1) to give a yellowish thick oil which was crystallized from absolute ethanol to give a white solid; m.p. 135°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04880804 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-6fbc542354b249f29e5a898a781a51d8 |
| Source note | uspto-grants-1989_11 |