Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442232Generated: October 27, 2026

Hydrochloric Acid → 1-methyl-4-(8H-dibenzo[a,e]furo[3,4-c]cyclohepten-8-ylidene)-piperidine

https://huagongshe.com/reaction/442232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,3,4,5-Tetraphenyl-2,4-cyclopentadien-1-oneHCID 68068—
Reactant1-methyl-4-(1,4-dihydro-1,4-epoxy-9H-tribenzo[a,c,e]cyclohepten-9-ylidene)-piperidineHCID 12368883—
SolventO-XyleneHCID 7237—
Product1-methyl-4-(8H-dibenzo[a,e]furo[3,4-c]cyclohepten-8-ylidene)-piperidineHCID 12368886—

Reaction Steps

To a solution of 3.20 g. (0.0093 mole) of 1-methyl-4-(1,4-dihydro-1,4-epoxy-9H-tribenzo[a,c,e]cyclohepten-9-ylidene)-piperidine in 105 ml. of xylene (b.p. 139°-140°) is added 3.60 g. (0.00936 mole) of tetraphenylcyclopentadienone ("tetracyclone"). The solution is stirred and refluxed for 22 hours. To the cooled solution is added 100 ml. of 3N hydrochloric acid. The crystalline solid that forms is removed by filtration and is washed thoroughly with benzene and ether. The white crystalline solid is dissolved in warm water and is treated with a solution of sodium carbonate. The resulting precipitate is extracted into benzene, washed with water, dried over magnesium sulfate, filtered, and the benzene is removed on a rotary evaporator. The crystalline residue, weighing 2.62 gm., is recrystallized from absolute methanol to give 1-methyl-4-(8H-dibenzo[a,e]furo[3,4-c]cyclohepten-8-ylidene)-piperidine, m.p. 147°-148°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044143
Source datasetuspto-grants-1977_08
ORD IDord-ec043dc558414d09a5a5d9d9150827b2
Source noteuspto-grants-1977_08