HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453540Generated: October 29, 2026
Hydrochloric Acid → methyl 2-bromo-3-(2-butyn-1-yl)-5-formyl-3H-imidazole-4-carboxylate
https://huagongshe.com/reaction/1453540
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | dimethyl 2-bromo-1-(but-2-ynyl)-1H-imidazole-4,5-dicarboxylate | HCID 21947677 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 2-bromo-3-(2-butyn-1-yl)-5-formyl-3H-imidazole-4-carboxylate | HCID 21947682 | — |
Reaction Steps
43 ml of a 1 M solution of diisobutylaluminium hydride in tetrahydrofuran are added dropwise within 20 minutes to a solution of 13.5 g of dimethyl 2-bromo-1-(2-butyn-1-yl)-1H-imidazole-4,5-dicarboxylate in 220 ml of tetrahydrofuran under an argon atmosphere at −70° C. The mixture is stirred for a further four hours at −70° C., then 20 ml of a mixture of 1 M hydrochloric acid and tetrahydrofuran are added dropwise. After heating to ambient temperature approx. 200 ml of water are added and the mixture is extracted three times with 70 ml of ethyl acetate. The combined extracts are dried and evaporated down. The crude product thus obtained is purified by column chromatography through silica gel with petroleum ether/ethyl acetate (4:1->1:1) as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476671B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-a93d0b1832a04492bfb8c25227319efe |
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| Source note | uspto-grants-2009_01 |
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