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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386783Generated: October 31, 2026

Hydrochloric Acid → 5-Bromo-1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-one

https://huagongshe.com/reaction/2386783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantDimethylacetamideHCID 31374—
Reactant5-Bromo-1,3-dihydro-2H-benzimidazol-2-oneHCID 12228060—
ReactantPotassium tert-butoxideHCID 23665647—
Product5-Bromo-1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-oneHCID 47003447—

Reaction Steps

Iodomethane (2.41 g) was added to a suspension of 5-bromo-1,3-dihydro-benzoimidazol-2-one (1.65 g) and potassium tert-butoxide (1.91 g) in DMA (20 ml). The mixture was stirred overnight at room temperature. The mixture was poured to 2.5N aqueous HCl (80 ml) and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and then concentrated in vacuo. Heptane (50 ml) was added to the residue and the mixture was filtered. The residue was washed with diethyl ether and dried in vacuo to give the title compound (1.1 g) as a light brown solid. MS (m/e)=241.1 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268820B2
Source datasetuspto-grants-2012_09
ORD IDord-fee2e925739c48ef8a0c41283ff96c9f
Source noteuspto-grants-2012_09