Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206443Generated: November 1, 2026

Hydrochloric Acid → HCID 178448596, compound

https://huagongshe.com/reaction/2206443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantFormaldehydeHCID 712—
ReactantButylamineHCID 8007—
ReactantSodium TetraphenylborateHCID 2723787—
Reactant(4-Methylphenyl)(pyridin-2-yl)methanoneHCID 3018781—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 178448596HCID 17844859672%

Reaction Steps

was prepared according to general procedure (A), in which 25 μl n-butylamine (0.25 mmol, 1 equiv), 28 μl formalin (0.37 mmol, 1.5 equiv), 82 μl 3.05 M hydrochloric acid in ethanol (0.25 mmol, 1 equiv) and 49 mg pyridin-2-yl(p-tolyl)methanone (0.25 mmol, 1 equiv) were combined in 0.50 mL acetonitrile and maintained at room temperature for 12 hours. The crude material was then dissolved in 1.0 mL methanol and then 94 mg sodium tetraphenylborate (0.27 mmol, 1.1 equiv) in 1.0 mL methanol was added drop wise while stirring vigorously. The heterogeneous mixture was stirred vigorously for 3 hours at room temperature until the solid became a fine suspension, which was then filtered, washed with 500 μl of methanol and dried under high vacuum at 0.2 Torr to obtain 105 mg 2-butyl-1-(p-tolyl)-2H-imidazo[1,5-a]pyridin-4-ium tetraphenylborate (0.18 mmol, a 72% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371448B2
Source datasetuspto-grants-2016_06
ORD IDord-be05a3522839429a8713492dac078490
Source noteuspto-grants-2016_06