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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580598Generated: October 25, 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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propenoyl chloride, 3-(3,4,5-trimethoxyphenyl)-, (2E)-HCID 112094—
Reactant10-hydroxy-2,3,11-trimethoxy-5,6,13,13a-tetrahydro-8H-dibenzo[a, g]quinolizine hydrochlorideHCID 86732983—
SolventPyridineHCID 1049—
Product5,6,13,13a-tetrahydro-2,3,11-trimethoxy-10-(3', 4', 5'-trimethoxycinnamoyloxy)-8H-dibenzo[a, g]quinolizineHCID 8673298546.4%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03933826
Source datasetuspto-grants-1976_01
ORD IDord-47292063710140caa1214a1d5fff1ce6
Source noteuspto-grants-1976_01