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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 427140Erstellt: 24. Oktober 2026

Ethyl bromoacetate → 3-Benzoyloxy-6,7-dimethoxy-9-carbethoxymethyl-1,2,3,4-tetrahydrocarbazole

https://huagongshe.com/de/reaction/427140

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
EduktSodium hydrideHCID 24758—
Edukt3-Benzoyloxy-6,7-dimethoxy-1,2,3,4-tetrahydrocarbazoleHCID 12891777—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Benzoyloxy-6,7-dimethoxy-9-carbethoxymethyl-1,2,3,4-tetrahydrocarbazoleHCID 12891850—

Reaktionsschritte

The 3-benzoyloxy-6,7-dimethoxy-9-carbethoxymethyl-1,2,3,4-tetrahydrocarbazole was prepared by following an alkylation procedure similar to that described in Example 11 but using 17.6 g. of 3-benzoyloxy-6,7-dimethoxy-1,2,3,4-tetrahydrocarbazole (see Example 4) and 2.14 g. of sodium hydride (56% in mineral oil) in 200 ml. of dimethylformamide, and 8.4 g. of ethyl bromoacetate. The crude product in ethyl acetate was filtered through alumina, the filtrate was evaporated to dryness under reduced pressure and the residue was recrystallized from ethyl acetate to give 3-benzoyloxy-6,7-dimethoxy-9-carbethoxymethyl-1,2,3,4-tetrahydrocarbazole, m.p. 125°-127° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04172834
Quelldatensatzuspto-grants-1979_10
ORD IDord-c2d91b91440840d594899d8b5ff9a084
Quellennotizuspto-grants-1979_10