HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740434Generated: October 31, 2026
Imidazole → 3-(1-Imidazolyl)-benzaldehyde dimethyl acetal
https://huagongshe.com/reaction/1740434
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-3-(dimethoxymethyl)benzene | HCID 105395 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(1-Imidazolyl)-benzaldehyde dimethyl acetal | HCID 22117824 | 79.4% |
Reaction Steps
A solution of 296 mg of imidazole and 131 mg of sodium hydride (80% dispersion in mineral oil) in 2 ml of anhydrous dimethylformamide was stirred at room temperature for 1 hour under nitrogen. 1.0 g of 3-bromobenzaldehyde dimethyl acetal and 30 mg copper powder were then added and the mixture was stirred at 150-160° C. under nitrogen for 36 hours. The cooled mixture was diluted with 20 ml of water and extracted with four 25 ml portions of dichloromethane. The combined extracts were washed with two 25 ml portions of 25% aqueous ammonia, followed by two 25 ml portions of brine and then dried over anhydrous magnesium sulphate. The solution was concentrated under reduced pressure to give 0.75 g of 3-(1-imidazolyl)-benzaldehyde dimethyl acetal as a clear viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05969139 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-b8d2021883814275bd64abc29882abf0 |
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| Source note | uspto-grants-1999_10 |
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