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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728413Generated: October 29, 2026

Imidazole → HCID 53673103, compound

https://huagongshe.com/reaction/1728413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTetrahydrofuranHCID 8028—
ReactantVinyloxiraneHCID 13586—
CatalystPalladiumHCID 23938—
ProductHCID 53673103HCID 5367310395%
ProductHCID 54181380HCID 541813805%

Reaction Steps

Reaction of 3,4-epoxy-1-butene and imidazole 1.95 g (0.0286 moles) of imidazole and 2.0 g (0.0286 moles) of 3,4-epoxy-1-butene were dissolved in 25 ml of THF. 0.83 g of the polymer-bound palladium(0) catalyst of Example 2 was then added to the reaction mixture. The reaction mixture was stirred at room temperature for 24 hours. The catalyst was removed by filtration and the filtrate was concentrated at reduced pressure. The residue was distilled. The reaction Yielded about 95% 4-(1-imidazoYl)-2-buten-1-ol (1,4 adduct) and less than 5% 3-(1-imidazoyl)-1-buten-4-ol (1,2 adduct). The combined yield of products was 63%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05326873
Source datasetuspto-grants-1994_07
ORD IDord-dfe18114c91d404484eb63a60e25a99b
Source noteuspto-grants-1994_07