HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324971Erstellt: 24. Oktober 2026
Triethylamine → 3-Phenyl[(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)methyl]benzene
https://huagongshe.com/de/reaction/324971
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Phenyl-1,2,3,6-tetrahydropyridine hydrochloride | HCID 2723860 | — |
| Edukt | 3-(Chloromethyl)-1,1'-biphenyl | HCID 15480892 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 3-Phenyl[(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)methyl]benzene | HCID 15521233 | — |
Reaktionsschritte
To a solution of 45 mg of 3-chloromethylbiphenyl in 5 mL of chloroform was added 50 mg of 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride and 0.5 mL triethylamine. The reaction mixture was heated at reflux temperature overnight, cooled to room temperature, washed successively with 50 mL aliquots of dilute sodim hydroxide and brine. The chloroform was removed by evaporation under reduced pressure to yield 3-phenyl[(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)methyl]benzene which was purified by chromatography on silica gel using 5% methanol in dichloromethane as eluent. Evaporation of the solvent yielded a solid which was treated with ethereal-HCl to give 15 mg of 3-[(4-1,2,3,6-tetrahydropyridin-1-yl)methyl]biphenyl hydrochloride (Compound 3), mp 236-238° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06221871B1 |
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| Quelldatensatz | uspto-grants-2001_04 |
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| ORD ID | ord-acaf77bd750842c2b73e4547080875d9 |
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| Quellennotiz | uspto-grants-2001_04 |
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