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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308841Generated: October 27, 2026

Maleic Acid → 1-[2-(4,5,10,11-tetrahydro-1H-dibenzo[a,d]cyclohepten-5-yl)ethyl]pyrrolidine maleate

https://huagongshe.com/reaction/2308841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AcidHCID 444266—
Reactant1-[2-(4,5,10,11-tetrahydro-1H-dibenzo[a,d]cyclohepten-5-yl)ethyl]pyrrolidineHCID 20187929—
SolventAcetoneHCID 180—
SolventHexaneHCID 8058—
Product1-[2-(4,5,10,11-tetrahydro-1H-dibenzo[a,d]cyclohepten-5-yl)ethyl]pyrrolidine maleateHCID 70432128—

Reaction Steps

660 g of crude 1-[2-(4,5,10,11-tetrahydro-1H-dibenzo[a,d]cyclohepten-5-yl)ethyl]pyrrolidine are dissolved in 3.0 l of acetone under an argon atmosphere while warming slightly (to about 40°). The solution obtained is cooled to about 10° and treated while stirring with a solution, pre-cooled to about 10°, of 264.0 g of maleic acid in 1.6 l of acetone and diluted with 4.0 l of n-hexane while passing argon through the mixture. After 15 hours at room temperature and with the exclusion of light, the resulting crystal slurry is filtered under suction, washed twice with 1.0 l of petroleum ether each time and dried at room temperature in a vacuum drying oven for 20 hours. There is obtained 1-[2-(4,5,10,11-tetrahydro-1H-dibenzo[a,d]cyclohepten-5-yl)ethyl]pyrrolidine maleate of melting point 127°-129°. By concentration of the mother liquor to about 1 l there is obtained a section portion of melting point 123° -125°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04691040
Source datasetuspto-grants-1987_09
ORD IDord-10b438af9c014bd2952d784baecf0f02
Source noteuspto-grants-1987_09