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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442234Generated: October 26, 2026

Hydrochloric Acid → HCID 12368887, compound

https://huagongshe.com/reaction/442234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,3,4,5-Tetraphenyl-2,4-cyclopentadien-1-oneHCID 68068—
Reactant1-methyl-4-(1-methyl-1,4-dihydro-1,4-epoxy-9H-tribenzo[a,c,e]cyclohepten-9-ylidene)piperidineHCID 12368885—
SolventO-XyleneHCID 7237—
ProductHCID 12368887HCID 12368887—

Reaction Steps

To a solution of 2.00 g. (0.00545 mole) of 1-methyl-4-(1-methyl-1,4-dihydro-1,4-epoxy-9H-tribenzo[a,c,e]cyclohepten-9-ylidene)piperidine and 2.16 g. (0.0056 mole) of tetraphenylcyclopentadienone in 60 ml. of xylene (b.p. 139°-140°) is stirred and refluxed for 20 hours. After cooling, 30 ml. of 6N hydrochloric acid is added. The precipitate that forms is removed by filtration and the solid precipitate is washed with ether and benzene. The solid is collected and made basic with 40% sodium hydroxide solution. The mixture is extracted with ether, and the ether extract is washed with water and dried over magnesium sulfate. After filtration, the ether is removed to give a crystalline residue which is recrystallized from methanol to give 1-methyl-4-(1-methyl-8H-dibenzo[a,e]furo[3,4-c]cyclohepten-8-ylidene)piperidine, m.p. 80°-86°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044143
Source datasetuspto-grants-1977_08
ORD IDord-d5d36e5f5746468588a98ff9adac1be1
Source noteuspto-grants-1977_08