HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370553Generated: October 26, 2026
Acetic Acid → 4-[(acetyloxy)methyl]-1,3-dihydro-5-(4-methoxybenzoyl)-2H-imidazol-2-one
https://huagongshe.com/reaction/370553
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-(bromomethyl)-1,3-dihydro-5-(4-methoxybenzoyl)-2H-imidazol-2-one | HCID 12856034 | — |
| Catalyst | Silver acetate | HCID 11246 | — |
| Catalyst | Silver bromide | HCID 66199 | — |
| Product | 4-[(acetyloxy)methyl]-1,3-dihydro-5-(4-methoxybenzoyl)-2H-imidazol-2-one | HCID 13477225 | — |
Reaction Steps
5-(Bromomethyl)-1,3-dihydro-4-(4-methoxybenzoyl)-2H-imidazol-2-one (3.1 g) is dissolved in 80 ml of acetic acid by warming on a steam bath. The solution obtained is allowed to cool to about 25°-45° C. and 1.7 g of silver acetate is added. The mixture is stirred at 25° C. for 16 hours and the precipitate which forms (silver bromide) is removed by filtration. The filtrate is concentrated to about 10 ml and a solid crystallizes. This is separated by filtration and recrystallized from acetic acid to give 4-[(acetyloxy)methyl]-1,3-dihydro-5-(4-methoxybenzoyl)-2H-imidazol-2-one melting at about 155°-162° C. This compound has the following structural formula: ##STR7##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04526981 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-b352a1b7a6e44e7789fb391720e00d48 |
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| Source note | uspto-grants-1985_07 |
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