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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270358Generated: November 1, 2026

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

https://huagongshe.com/reaction/1270358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 178517141HCID 178517141—
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 DM (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 numberUS07202251B2
Source datasetuspto-grants-2007_04
ORD IDord-c0e39f8c3fd44e8dbdb5165aedf4466d
Source noteuspto-grants-2007_04