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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1290319Erstellt: 26. Oktober 2026

Diethyl Malonate → Diethyl 2-(1-Bromo-2-naphthylmethyl)malonate

https://huagongshe.com/reaction/1290319

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl MalonateHCID 7761—
Edukt1-Bromo-2-(bromomethyl)naphthaleneHCID 37828—
EduktSodium ethoxideHCID 2723922—
EduktSodiumHCID 5360545—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktDiethyl 2-(1-Bromo-2-naphthylmethyl)malonateHCID 1449149295,6%

Reaktionsschritte

To a solution of NaOEt prepared from 9.66 g of sodium and 210 mL of dry EtOH was added 63.76 mL of diethyl malonate and the reaction mixture refluxed for 2 h. To the resulting yellow solution was added in small portions 126 g of 1-bromo-2-bromomethylnaphthalene and the reaction mixture refluxed for 16 h. Distillation of ethanol from an oil bath (100°-110° C.) through a simple Claisen head gave a yellow suspension, to which was added 350 mL of CH2Cl2 and 350 mL of H2O. The aqueous layer was extracted twice with 120-mL portions of CH2Cl2, and the combined organic layer was washed three times with 100-mL portion of H2O, dried (MgSO4) and evaporated to give 152 g (95.6%) of the ester as a yellow solid, mp 60°-65° C. Recrystallization from acetic acid gave 137 g (86.2%) of the pure diester as a colorless solid, mp 77°-79° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05750767
Quelldatensatzuspto-grants-1998_05
ORD IDord-edce69a42435422ba59d585e8c0d274a
Quellennotizuspto-grants-1998_05