Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251006Generated: October 31, 2026

Ammonium formate → 1-(4,4-Dimethoxy-butyl)-3-hydroxy-imidazolidin-2-one

https://huagongshe.com/reaction/251006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-Benzyloxy-3-(4,4-dimethoxy-butyl)-imidazolidin-2-oneHCID 67272508—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(4,4-Dimethoxy-butyl)-3-hydroxy-imidazolidin-2-oneHCID 6727234566%

Reaction Steps

To a solution of 1-Benzyloxy-3-(4,4-dimethoxy-butyl)-imidazolidin-2-one (1.61 g, 5.22 mmol) in EtOH (50 mL) was added ammonium formate (3.34 g, 52.9 mmol) and 10 wt % Pd/C (50% wet with water, 800 mg) and the mixture was stirred at room temperature for 2 hours. The mixture was vacuum filtered through celite and the cake was washed with EtOH. The solvent was removed from the filtrate under reduced pressure and the thus obtained solid was partitioned between water (10 mL) and CH2Cl2 (50 mL). The phases were separated and the aqueous phase was extracted with CH2Cl2 (3×10 mL). The combined organic extracts were dried (Na2SO4) and concentrated. Purification of the crude material by column chromatography on silica gel (100% EtOAc) provided 0.75 g (66%) of 1-(4,4-Dimethoxy-butyl)-3-hydroxy-imidazolidin-2-one as a colorless oil. ES-MS m/z 241 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863293B2
Source datasetuspto-grants-2011_01
ORD IDord-61809e737566463f829330d5f8a38c37
Source noteuspto-grants-2011_01