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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 736790Erstellt: 25. Oktober 2026

Sodium Iodide → methyl 1-(10,11-dihydro5H-dibenzo[a,d][7]annulen-5-yl)-1,2,5,6-tetrahydropyridine-3-carboxylate

https://huagongshe.com/reaction/736790

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktTriethylamineHCID 8471—
Edukt5H-Dibenzo(a,d)cycloheptene, 10,11-dihydro-5-chloro-HCID 14587—
EduktNorarecoline HydrochlorideHCID 201540—
Lösungsmittel1,4-DioxaneHCID 31275—
Produktmethyl 1-(10,11-dihydro5H-dibenzo[a,d][7]annulen-5-yl)-1,2,5,6-tetrahydropyridine-3-carboxylateHCID 6881668255%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of methyl 1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride (crude, 150 mmol), 5-chlorodibenzosuberane (41 g, 180 mmol, 1.2 eq), sodium iodide (2.2 g, 15 mmol, 0.1 eq) and triethylamine (63 mL, 450 mmol, 3.0 eq) in dioxane (300 mL) was stirred at 90° C. overnight. The reaction mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, and concentrated. The crude product was passed through a silica gel plug, eluting with CH2Cl2. After concentration, the resulting solid was triturated with ether to yield 27 g (55%) of methyl 1-(10,11-dihydro5H-dibenzo[a,d][7]annulen-5-yl)-1,2,5,6-tetrahydropyridine-3-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595327B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-7faa392ab5ba428d8d9d7037bc35f0ee
Quellennotizuspto-grants-2009_09