HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206443Generated: November 1, 2026
Hydrochloric Acid → HCID 178448596, compound
https://huagongshe.com/reaction/2206443
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Sodium Tetraphenylborate | HCID 2723787 | — |
| Reactant | (4-Methylphenyl)(pyridin-2-yl)methanone | HCID 3018781 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178448596 | HCID 178448596 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09371448B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-be05a3522839429a8713492dac078490 |
|---|
| Source note | uspto-grants-2016_06 |
|---|