HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592439Generated: October 29, 2026
Ammonium formate → 1-(4,4-Dimethoxy-butyl)-3-hydroxy-imidazolidin-2-one
https://huagongshe.com/reaction/1592439
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1-Benzyloxy-3-(4,4-dimethoxy-butyl)-imidazolidin-2-one | HCID 67272508 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4,4-Dimethoxy-butyl)-3-hydroxy-imidazolidin-2-one | HCID 67272345 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291631B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-2d82f05ff2c9436cbdb04567c3e17f79 |
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| Source note | uspto-grants-2007_11 |
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