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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16575Erstellt: 24. Oktober 2026

Bis(2-bromoethyl) ether → Tert-butyl 4-cyanooxane-4-carboxylate

https://huagongshe.com/de/reaction/16575

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis(2-bromoethyl) etherHCID 21521—
EduktSodium hydrideHCID 24758—
Edukttert-Butyl cyanoacetateHCID 70693—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl 4-cyanooxane-4-carboxylateHCID 2313161057%

Reaktionsschritte

To a stirred suspension of NaH (17.7 g, 0.443 mol) in DMF (200 mL) was added dropwise tert-butyl cyanoacetate (25.0 g, 0.177 mol) in DMF (100 mL) at 0° C. under N2. The mixture was allowed to warm to ambient temperature, and stirred for 1 hour. Then, bis(2-bromoethyl)ether (49.3 g, 0.177 mol) was added to the mixture, and the resulting mixture was stirred at 90° C. for 24 h. After cooling to 0° C., the mixture was quenched with water (100 mL). The volatile components were removed by evaporation and the residue was precipitated with a mixture of EtOAc-Toluene (1:2, 500 mL) and water (500 mL). The organic phase was washed with water (500 mL) for three times, dried over Na2SO4, filtered and evaporated. The solid was washed with Hexane and dried in vacuo to give 19.0 g (57%) of the title compound as a white crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737163B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-f69d8475eee74539846885ab791bd680
Quellennotizuspto-grants-2010_06