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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 1-[2-(4,5,10,11-tetrahydro-1H-dibenzo[a,d]cyclohepten-5-yl)ethyl]pyrrolidine | HCID 20187929 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-[2-(4,5,10,11-tetrahydro-1H-dibenzo[a,d]cyclohepten-5-yl)ethyl]pyrrolidine maleate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04691040 |
|---|
| Source dataset | uspto-grants-1987_09 |
|---|
| ORD ID | ord-10b438af9c014bd2952d784baecf0f02 |
|---|
| Source note | uspto-grants-1987_09 |
|---|