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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116776Generated: October 30, 2026

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

https://huagongshe.com/reaction/2116776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactantdimethyl 2-bromo-1-(3-methyl-2-buten-1-yl)-1H-imidazole-4,5-dicarboxylateHCID 59815068—
SolventTetrahydrofuranHCID 8028—
Productmethyl 2-bromo-3-(3-methyl-2-buten-1-yl)-5-formyl-3H-imidazole-4-carboxylateHCID 11580300—

Reaction Conditions

Temperature-65 °C

Reaction Steps

Under an argon atmosphere 35 ml (35 mmol) diisobutylaluminium hydride (1 mol/l in toluene) were added dropwise at −65° C. within 20 minutes to a solution of 9.00 g (12.18 mmol) dimethyl 2-bromo-1-(3-methyl-2-buten-1-yl)-1H-imidazole-4,5-dicarboxylate in 140 ml of tetrahydrofuran. After 1 hour at −65° C. another 5 ml (5 mmol) diisobutylaluminium hydride (1 mol/l in toluene) was added dropwise. The mixture was stirred for a further hour at −65° C. and then 20 ml of a 1:1 mixture of hydrochloric acid (1 mol/l) and tetrahydrofuran were added dropwise. After heating to ambient temperature approx. 100 ml of water was added, and the mixture was extracted three times with 70 ml of ethyl acetate. The extracts were dried over sodium sulphate, evaporated down, and the crude product thus obtained was purified by column chromatography (silica gel; eluant: cyclohexane/ethyl acetate 3:1->1:2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439370B2
Source datasetuspto-grants-2008_10
ORD IDord-d92ef697781746b294acef8bc5ae9889
Source noteuspto-grants-2008_10