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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1605954Erstellt: 25. Oktober 2026

Ethyl chloroformate → 2-Benzyl-5-carbethoxy-2,5-diazabicyclo[2.2.1]heptane

https://huagongshe.com/reaction/1605954

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl chloroformateHCID 10928—
Edukt2-benzyl-5-(N,N-diethyl-carbamyl)2,5-diazabicyclo[2.2.1]heptane hydrochlorideHCID 21545496—
Edukt2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydroiodideHCID 22403956—
Produkt2-Benzyl-5-carbethoxy-2,5-diazabicyclo[2.2.1]heptaneHCID 2209953468%

Reaktionsschritte

Using the procedure for preparation of 2-benzyl-5-(N,N-diethylcarbamyl)-2,5-diazabicyclo[2.2.1]heptane hydrochloride as related in Example 11, 29.0 g of 2-benzyl-2,5-diazabicyclo[2.2.1]heptane dihydroiodide, prepared according to the procedure given in Example 11, was treated with 1.5 equivalents of ethyl chloroformate to yield crude product. Dry column chromatography, a technique described by B. Loev and M. M. Goodman in Chem. Ind. (London), p 2026, 1967, on 1700 g alumina using chloroform development provided 11.6 g (68%) of pure product, characterized as the maleate salt, melting point 124°-128° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03951980
Quelldatensatzuspto-grants-1976_04
ORD IDord-f7c2ba8b83ac4f5f9885995a3e0add35
Quellennotizuspto-grants-1976_04