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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643983Generated: October 31, 2026

tert-Butyl 2-bromobutanoate → HCID 66755153, compound

https://huagongshe.com/reaction/1643983

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 2-bromobutanoateHCID 13124118—
Reactant5-Cyano-2-oxo-2,3-dihydro-benzoimidazole-1-carboxylic acid tert-butyl esterHCID 24900958—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 66755153HCID 6675515372.1%

Reaction Steps

To a chilled solution of 5-cyano-2-oxo-2,3-dihydro-benzoimidazole-1-carboxylic acid tert-butyl ester (50 mg, 0.19 mmol) in dry DMF (1 mL) NaH (60% dispersion mineral oil, 8 mg, 0.20 mmol) was added under N2 atmosphere. The reaction was stirred at room temperature for 15 min. Then, a solution of tert-butyl-2-bromobutyrate (0.054 mL, 0.29 mmol) in DMF (2 mL) was added at 0° C. The reaction mixture was stirred at room temperature for 3 hours, diluted with ethyl acetate, washed with water, with a saturated NH4Cl aqueous solution, brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography in silical gel using 15% ethyl acetate in n-heptane as eluent to afford 3-(1-tert-butoxycarbonyl-propyl)-5-cyano-2-oxo-2,3-dihydro-benzoimidazole-1-carboxylic acid tert-butyl ester (55 mg, 72%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119676B2
Source datasetuspto-grants-2012_02
ORD IDord-d167748901c84a45b64c1663f511e3f2
Source noteuspto-grants-2012_02