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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899873Generated: November 1, 2026

Hydrochloric Acid → HCID 57127353, compound

https://huagongshe.com/reaction/1899873

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 1M 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 1N 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 numberUS05574046
Source datasetuspto-grants-1996_11
ORD IDord-f2aadb00bb9849749182cb21406543b3
Source noteuspto-grants-1996_11