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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501394Generated: October 29, 2026

Hydrochloric Acid → HCID 23070903, compound

https://huagongshe.com/reaction/501394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23070878HCID 23070878—
CatalystMercuric acetateHCID 15337—
SolventEthyl AcetateHCID 8857—
ProductHCID 23070903HCID 2307090325.5%

Reaction Steps

0.187 g of mercury (II) acetate and 0.090 of sodium borohydride were added to 8 ml of an ethanol solution containing 0.265 g of t-butyl 4-[1-(2-butynyl)-5-ethoxycarbonyl-4-methylsulfanyl carbonyl-1H-imidazol-2-yl]piperazine-1-carboxylate at 0° C., and the mixture was stirred at room temperature for 4 hours. After 0.187 g of mercury (II) acetate and 0.090 of sodium borohydride had been added to the solution, the mixture was stirred at room temperature for 15 hours. 100 ml of ethyl acetate and 50 ml of 0.5N hydrochloric acid were added to the solution, and the organic layer was washed successively with 50 ml of water and 50 ml of a saturated sodium chloride solution. The mixture was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography. 0.172 g of the starting material was collected from the fraction eluted with hexane-ethyl acetate (4:1). Then, 0.061 g of the title compound was obtained from the fraction eluted with hexane-ethyl acetate (1:4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772226B2
Source datasetuspto-grants-2010_08
ORD IDord-aee4171ffd7f47a6ae020a6bd65b03f3
Source noteuspto-grants-2010_08