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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256683Generated: October 25, 2026

Hydrochloric Acid → Benzyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylate

https://huagongshe.com/reaction/256683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylateHCID 15640822—
CatalystTitanium(IV)ethoxideHCID 2724286—
SolventBenzyl AlcoholHCID 244—
SolventWaterHCID 962—
ProductBenzyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylateHCID 18957067143.5%

Reaction Steps

A solution of 1.62 9 of tetraethyl orthotitanate in 71 ml of benzyl alcohol was treated with 4.52 g of methyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylate and stirred at 115°-120° under argon for 3 hours. The reaction mixture was then cooled, stirred with 71 ml of 1N hydrochloric acid for 1 hour, diluted with 350 ml of water and extracted several times with methylene chloride. The organic phases were washed with saturated sodium hydrogen carbonate solution, dried over sodium sulphate, filtered and evaporated. The residue was stirred in 710ml of diethyl ether for 1 hour, suction filtered and the material obtained was dried in a vacuum. There was obtained 4.02g of benzyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylate as yellowish crystals with a m.p. of 229°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258387
Source datasetuspto-grants-1993_11
ORD IDord-21cb10d88c6e42f7b4b0e618b702c92c
Source noteuspto-grants-1993_11