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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675747Generated: October 31, 2026

Sodium hydride → Tert-butyl (2-oxo-2,3-dihydrobenzimidazol-1-yl)acetate

https://huagongshe.com/reaction/1675747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 178517141HCID 178517141—
SolventDimethylformamideHCID 6228—
ProductTert-butyl (2-oxo-2,3-dihydrobenzimidazol-1-yl)acetateHCID 20814117—

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003792B2
Source datasetuspto-grants-2011_08
ORD IDord-1026f8032d624022b224cd2514c6e956
Source noteuspto-grants-2011_08