HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274532Generated: October 27, 2026
Triethylamine → 1-[(Benzyloxy)methyl]imidazol-2-yl (3,4-dimethoxy-5-nitrophenyl) ketone
https://huagongshe.com/reaction/274532
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Benzyloxymethylimidazole | HCID 14795908 | — |
| Reactant | 3,4-Dimethoxy-5-nitrobenzoyl chloride | HCID 21928615 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[(Benzyloxy)methyl]imidazol-2-yl (3,4-dimethoxy-5-nitrophenyl) ketone | HCID 19000172 | — |
Reaction Steps
A solution of 10.0 g of 1-[(benzyloxy)- methyl]imidazole in 50 ml of acetonitrile is added dropwise within 10 minutes while cooling with ice to a solution of 13.0 g of 3,4-dimethoxy-5-nitrobenzoyl chloride and 5.4 g of triethylamine in 80 ml of acetonitrile so that the temperature does not exceed 25° . The mixture is subsequently stirred for an additional 3 hours, whereupon the solvent is distilled. After treatment with water, the mixture is extracted with ethyl acetate. After two-fold washing with water, the organic phase is dried over sodium sulfate and evaporated. The resulting oil is chromatographed on 600 g of silica gel with toluene/ethyl acetate (95:5). There is obtained 1-[(benzyloxy)methyl]imidazol-2-yl (3,4-dimethoxy-5-nitrophenyl) ketone as a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05389653 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-04cc483c3e344de4b3a61033c0a61542 |
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| Source note | uspto-grants-1995_02 |
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