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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Chloro-1-(1-chloro-ethyl)-4-methoxy-benzene | HCID 61083462 | — |
| Reactant | 1,3-Diallyl-2-oxo-2,3-dihydro-1H-benzoimidazole-5-carboxylic acid methoxy-methyl-amide | HCID 86645878 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Diallyl-5-[2-(2-chloro-4-methoxy-phenyl)-propionyl]-1,3-dihydro-benzoimidazol-2-one | HCID 66697350 | 52.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268820B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-9feceda733b8490ba6511fca1c77d752 |
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| Source note | uspto-grants-2012_09 |
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