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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698555Generated: November 1, 2026

Hydrochloric Acid → 7-(1-Ethylpropyl)-1-methyl-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1698555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant7-(1-Ethyl-1-hydroxypropyl)-1-methyl-1,3-dihydro-2H-benzimidazol-2-oneHCID 67273488—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product7-(1-Ethylpropyl)-1-methyl-1,3-dihydro-2H-benzimidazol-2-oneHCID 6727261354%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 7-(1-ethyl-1-hydroxypropyl)-1-methyl-1,3-dihydro-2H-benzimidazol-2-one (6.00 g, 25.6 mmol) and 6N HCl (20 mL) in ethanol (100 mL) was stirred at 50° C. for 3 h. The mixture was concentrated in vacuo, and the resulting residue was dissolved in ethyl acetate, washed with aqueous potassium carbonate. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo to give pale yellow oil, which was used in the next reaction without further purification. MS Calcd.: 216. Found: 217 (M+H). The crude material was dissolved in ethanol (150 mL). This solution was treated with 10% palladium on carbon (50% wet; 1.00 g), purged with hydrogen, and stirred under 5 atoms hydrogen for 7 h. The catalyst was removed by filtration and the filtrate was concentrated in vacuo. The residue was crystallized from ethanol/diethylether to afford the title compound as colorless crystals (3.02 g, 54%). mp 130-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163935B2
Source datasetuspto-grants-2012_04
ORD IDord-0bae978b80774283b4d94f32208c7ae6
Source noteuspto-grants-2012_04