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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386804Generated: October 30, 2026

Water → 1,3-Diallyl-5-[2-(2-chloro-4-methoxy-phenyl)-propionyl]-1,3-dihydro-benzoimidazol-2-one

https://huagongshe.com/reaction/2386804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMagnesiumHCID 5462224—
Reactant2-Chloro-1-(1-chloro-ethyl)-4-methoxy-benzeneHCID 61083462—
Reactant1,3-Diallyl-2-oxo-2,3-dihydro-1H-benzoimidazole-5-carboxylic acid methoxy-methyl-amideHCID 86645878—
SolventTetrahydrofuranHCID 8028—
Product1,3-Diallyl-5-[2-(2-chloro-4-methoxy-phenyl)-propionyl]-1,3-dihydro-benzoimidazol-2-oneHCID 6669735052.8%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A 1M suspension of Rieke magnesium in THF (1.3 ml) was added to THF (2 ml). The mixture was cooled to −10° C., and a solution of 2-chloro-1-(1-chloro-ethyl)-4-methoxy-benzene (136 mg) in THF (2 ml) was added. The mixture was stirred for 15 min. A solution of 1,3-diallyl-2-oxo-2,3-dihydro-1H-benzoimidazole-5-carboxylic acid methoxy-methyl-amide (100 mg) in THF (2 ml) was added at −10° C. The mixture was stirred overnight at room temperature. Water was added and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and then concentrated to an oil. The residue was purified by flash chromatography (SiO2, 0 to 100% EtOAc/heptane) to give the title compound (72 mg) as a light yellow foam. MS (m/e)=411.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268820B2
Source datasetuspto-grants-2012_09
ORD IDord-9feceda733b8490ba6511fca1c77d752
Source noteuspto-grants-2012_09