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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648552Generated: October 28, 2026

p-Toluenesulfonic acid → 4,5-dihydro-7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizine-10-carboxaldehyde

https://huagongshe.com/reaction/648552

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,3-DiethoxypropyneHCID 66285—
Reactant5,6-Dihydro-3-hydroxy-2-phenylthiazolo[3,2-a]thieno[2,3-c]pyridinium hydroxideHCID 14770017—
SolventCyclohexanoneHCID 7967—
Product4,5-dihydro-7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizine-10-carboxaldehydeHCID 14770038—

Reaction Steps

A mixture of 0.855 g of 5,6-dihydro-3-hydroxy-2-phenylthiazolo[3,2-a]thieno[2,3-c]pyridinium hydroxide (internal salt) and 0.65 ml of 3,3-diethoxypropyne in 30 ml of cyclohexanone was stirred with a few crystals of p-toluenesulfonic acid at 130° for 3 hours under an inert gas and then concentrated in vacuo. The residue was taken up in ethyl acetate, washed with 10 percent potassium bicarbonate solution and saturated sodium chloride solution, dried over magnesium sulfate, concentrated and chromatographed on silica gel with toluene/acetonitrile (19:1). By crystallization from dioxane, there is obtained 4,5-dihydro-7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizine-10-carboxaldehyde of m.p. 213°-215°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735940
Source datasetuspto-grants-1988_04
ORD IDord-9dc9d217395445a1aa883eed4bf48143
Source noteuspto-grants-1988_04