HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444748Generated: October 26, 2026
2-Fluorobiphenyl-4-carboxaldehyde → 3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride
https://huagongshe.com/reaction/1444748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluorobiphenyl-4-carboxaldehyde | HCID 2759083 | — |
| Reactant | 3-(5-Ammoniopentanoyl)pyridinium chloride | HCID 67337657 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride | HCID 67339152 | 73.8% |
Reaction Steps
3-(5-Ammoniopentanoyl)pyridinium chloride (150 mg, 0.60 mmol) and 2-fluorobiphenyl-4-carboxaldehyde (155 mg, 0.78 mmol) were combined in a reaction vessel and treated with ethanol (10 mL) and concentrated HCl(aq) (5 drops). The vessel was then sealed and the reaction was heated to 85° C. overnight then cooled to room temperature. The reaction mixture was then concentrated under reduced pressure then partially dissolved into hot isopropanol. This mixture was left to cool and crystals formed. The crystals were recovered by vacuum filtration, washed with fresh isopropanol, and dried under vacuum giving 92 mg (36%) of a yellow solid. LC-MS: RT=5.88 min, [M+H]+=343.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07662965B2 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-7de7f797cb24449bbe4a42e5c238b9f8 |
|---|
| Source note | uspto-grants-2010_02 |
|---|