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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090274Generated: October 25, 2026

Succinic Acid → Succinic Acid

https://huagongshe.com/reaction/2090274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic AcidHCID 1110—
ReactantIsopropanolHCID 3776—
ReactantSolifenacinHCID 154059—
ProductSuccinic AcidHCID 1110—
ProductSolifenacin SuccinateHCID 216457—

Reaction Steps

Crude oily solifenacin (35 g) obtained in Example 1 is dissolved in isopropanol (100 mL) at room temperature (20-24° C.). In a separate flask the solution of succinic acid (11.30 g, 95.55 mmol) in isopropanol (130 mL) is prepared at reflux for 5 min. The hot succinic acid solution is slowly added to the solifenacin solution in isopropanol. The resulting mixture is left to reach room temperature. At ca. 45° C. the mixture turned to be cloudy and white crystalline solid begins to precipitate. The solution is left at room temperature for 2 h 30 min. The crystalline solid is filtered off and washed with cold isopropanol (10° C.) (3×40 mL), then it is dried under reduced pressure (0.1-0.15 mmHg, room temperature, 2 h) to dry mass. After two steps solifenacin succinate is obtained in 38.9 g, (84.8%) yield, of purity (HPLC) 99.39%. The final product (38 g) is recrystallized in isopropanol (150 mL), yielding 34.4 g (90.7%) of solifenacin succinate of purity (HPLC) 99.71%; T(onset)≈150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436182B2
Source datasetuspto-grants-2013_05
ORD IDord-b54bb51777094ad4a4a18321e9a3e7fd
Source noteuspto-grants-2013_05