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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444747Generated: October 26, 2026

Hydrochloric Acid → 3-(3-(Biphenyl-4-ylmethylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride

https://huagongshe.com/reaction/1444747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(1,1'-Biphenyl)-4-carboxaldehydeHCID 76689—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium AcetateHCID 517045—
Reactant3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product3-(3-(Biphenyl-4-ylmethylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochlorideHCID 67338607—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-(5-Ammoniopentanoyl)pyridinium chloride (128 mg, 0.51 mmol) was suspended in methanol (2 mL) and treated with N,N-diisopropylethylamine (165 mg, 1.27 mmol) in a reaction vessel. This gave a clear solution. A dual solution of 0.6 M acetic acid and 0.3 M sodium acetate in methanol (10 mL) was then added, followed by addition of 4-phenylbenzaldehyde (140 mg, 0.76 mmol). The reaction vessel was then sealed and the reaction heated to 80 ° C. overnight then cooled to room temperature. The reaction mixture was then concentrated under reduced pressure, treated with a saturated solution of NaHCO3(aq), and extracted three times with EtOAc. The EtOAc extracts were washed with brine, then combined, dried over Na2SO4, filtered and concentrated under reduced pressure. The recovered material was eluted through a 20 gram column of silica gel with 7:7:7:1:0.1 hexane:MtBE:CH2Cl2:MeOH:NH4OH eluant. One sample was recovered and dried under vacuum. This sample was then dissolved into MeOH and treated with two equivalents of 6 N HCl(aq), concentrated under reduced pressure and re-crystallized from isopropanol giving 80 mg (39%) of yellow needles. LC-MS: RT=5.72 min, [M+H]+ =325.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662965B2
Source datasetuspto-grants-2010_02
ORD IDord-d43a3295814d480eb2cd3b064c639753
Source noteuspto-grants-2010_02