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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1580598Erstellt: 27. Oktober 2026

2-Propenoyl chloride, 3-(3,4,5-trimethoxyphenyl)-, (2E)- → 5,6,13,13a-tetrahydro-2,3,11-trimethoxy-10-(3', 4', 5'-trimethoxycinnamoyloxy)-8H-dibenzo[a, g]quinolizine

https://huagongshe.com/reaction/1580598

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Propenoyl chloride, 3-(3,4,5-trimethoxyphenyl)-, (2E)-HCID 112094—
Edukt10-hydroxy-2,3,11-trimethoxy-5,6,13,13a-tetrahydro-8H-dibenzo[a, g]quinolizine hydrochlorideHCID 86732983—
LösungsmittelPyridineHCID 1049—
Produkt5,6,13,13a-tetrahydro-2,3,11-trimethoxy-10-(3', 4', 5'-trimethoxycinnamoyloxy)-8H-dibenzo[a, g]quinolizineHCID 8673298546,4%

Reaktionsschritte

1.9 g of 10-hydroxy-2,3,11-trimethoxy-5,6,13,13a-tetrahydro-8H-dibenzo[a, g]quinolizine hydrochloride was treated in the same manner as described in Example 6, using 2.0 g of 3,4,5-trimethoxycinnamoyl chloride and 20 ml of anhydrous pyridine and there was obtained 1.3 g (46.4% yield) of 5,6,13,13a-tetrahydro-2,3,11-trimethoxy-10-(3', 4', 5'-trimethoxycinnamoyloxy)-8H-dibenzo[a, g]quinolizine as a pale yellow powder. The methiodide derived from this compound was found to be in agreement with the methiodide of the compound obtained in Example 5 as determined from the melting point and IR spectrum.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03933826
Quelldatensatzuspto-grants-1976_01
ORD IDord-47292063710140caa1214a1d5fff1ce6
Quellennotizuspto-grants-1976_01