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HRID 484334Erstellt: 24. Oktober 2026

Triethylamine → 1-(4-nitrophenyloxycarbonyl)-1,2,5,6-tetrahydropyridine-3-carboxaldehyde-O-methyloxime

https://huagongshe.com/de/reaction/484334

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-Nitrophenyl chloroformateHCID 82129—
Edukt1,2,5,6-Tetrahydropyridine-3-carboxaldehyde-O-methyloximeHCID 197313—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(4-nitrophenyloxycarbonyl)-1,2,5,6-tetrahydropyridine-3-carboxaldehyde-O-methyloximeHCID 307286395%

Reaktionsschritte

A solution of 97% 4-nitrophenyl chloroformate (1.5 g, 7.22 mmoles) in dichloromethane (15 mL) was added at 0° C. to a stirred solution of 1,2,5,6-tetrahydropyridine-3-carboxaldehyde-O-methyloxime (0.92 g, 6.6 mmoles) and triethylamine (0.92 mL, 6.6 mmoles) in dichloromethane (20 mL). The reaction mixture was then stirred at room temperature for 20 minutes, the solvent was evaporated and the residue was partitioned between water and ethyl acetate. The organic layer was dried (Na2SO4) and evaporated. The solid was recrystallized from benzene-cyclohexane to give 1.9 g (95%) of the desired product with mp 109°-110° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05231107
Quelldatensatzuspto-grants-1993_07
ORD IDord-fd4c77fa32594158be7a2ba968f393e8
Quellennotizuspto-grants-1993_07