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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955063Generated: November 1, 2026

Hydrochloric Acid → HCID 57127353, compound

https://huagongshe.com/reaction/1955063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Benzylpiperidine-4-carbaldehydeHCID 89584—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(1-ethyl-2-methylbenzimidazol-5-yl)ethanoneHCID 5173516—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57127353HCID 5712735326.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of 0.1 g (0.5 mM) of 1-ethyl-2-methylbenzimidazole-5-yl methyl ketone and 0.1 g (0.5 mM) 4-formyl-N-benzylpiperidine in 10 mL of tetrahydrofuran (THF) was cooled to -78° C. under a nitrogen atmosphere. To this mixture were added dropwise 0.5 mL (0.5 mM) of a IM solution of lithium bis(trimethylsilyl)amide in THF. The reaction was stirred at -78° C. for 1 hour, then warmed to room temperature. To the reaction was added 10 mL of water and the pH was adjusted to 2.0 with 1N hydrochloric acid (HCl). The mixture was extracted with 15 mL of ethyl acetate. The pH of the water layer was then sequentially adjusted to 3.0, 4.0, 5.0, 6.5, and 8.5 with IN NaOH, each time extracting with 15 mL of ethyl acetate. The ethyl acetate extracts at pH=5.0 and 6.5 were combined, dried with sodium sulfate (Na2SO4) and evaporated to yield 50 mg (26%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124321
Source datasetuspto-grants-2000_09
ORD IDord-9993d18ec7c24106b70ced67464d9a43
Source noteuspto-grants-2000_09