HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Tert-butyl (2-oxo-2,3-dihydrobenzimidazol-1-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | HCID 178517141 | HCID 178517141 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl (2-oxo-2,3-dihydrobenzimidazol-1-yl)acetate | HCID 20814117 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a stirred mixture of 2-hydroxybenzimidazole (4.00 g, 29.8 mmol) and tert-butyl bromoacetate (5.53 g, 28.3 mmol) in DMF (50 mL) at 0° C. was added sodium hydride (1.31 g of a 60% dispersion in mineral oil, 32.8 mmol). The mixture was stirred at 0° C. for 1 h, then quenched with saturated aqueous NaHCO3 and concentrated in vacuo. The residue was partitioned between EtOAc (500 mL) and H2O (300 mL) and the organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:EtOAc—100:0 to 0:100, to give the title compound. MS: m/z=249 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071771B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-3f616e7d4a1740cb9dc83a48d39e1273 |
| Source note | uspto-grants-2011_12 |