Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351077Generated: November 1, 2026

Hydrochloric Acid → methyl 2-bromo-3-(2-butyn-1-yl)-5-formyl-3H-imidazole-4-carboxylate

https://huagongshe.com/reaction/1351077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactantdimethyl 2-bromo-1-(but-2-ynyl)-1H-imidazole-4,5-dicarboxylateHCID 21947677—
SolventTetrahydrofuranHCID 8028—
Productmethyl 2-bromo-3-(2-butyn-1-yl)-5-formyl-3H-imidazole-4-carboxylateHCID 21947682—

Reaction Conditions

Temperature-70 °C

Reaction Steps

43 ml of a 1 M solution of diisobutyl-aluminium 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 1M 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 over silica gel with petroleum ether/ethyl acetate (80:20 to 50:50) as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217711B2
Source datasetuspto-grants-2007_05
ORD IDord-1d55cdc3e7b94fea8aff3cf2cc459776
Source noteuspto-grants-2007_05