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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249583Generated: October 31, 2026

Fumaric Acid → 3-[8-[4-(2,2-diphenylethenyl)-1-piperidinyl]octyl]pyridine (E)-2-butenedioate salt

https://huagongshe.com/reaction/1249583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFumaric AcidHCID 444972—
Reactant3-[8-[4-(2,2-Diphenylethenyl)-1-piperidinyl]octyl]pyridineHCID 13754506—
SolventEthanolHCID 702—
Product3-[8-[4-(2,2-diphenylethenyl)-1-piperidinyl]octyl]pyridine (E)-2-butenedioate saltHCID 1375450797%

Reaction Steps

A 2-L Erlenmeyer flask was charged with 205.5 g of 3-[8-[4-(2,2-diphenylethenyl)-1-piperidinyl]octyl]pyridine 420 mL of 2B ethanol, and 55.5 g (5% excess) of fumaric acid. The mixture was heated on a steam cone to solution and filtered through Celite into a 12-L flask equipped with a mechanical stirrer. The filter cake was washed with an additional 420 mL of warm 2B ethanol. The stirred filtrate was diluted rapidly with 5.10 L of acetone. Crystallization began within a few minutes. The suspension was cooled in an ice-acetone bath for 1.0 hour and filtered. The solid was washed with 2×1.0 L=2.0 L of cold acetone and dried in a forced air oven at 75° to give 249.9 g (97% yield) of 3-[8-[4-(2,2-diphenylethenyl)-1-piperidinyl]octyl]pyridine (E)-2-butenedioate salt as a white solid, mp 126°-127°. Lc showed this material to be homogeneous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632925
Source datasetuspto-grants-1986_12
ORD IDord-3eb09357a836423999e8d15aa7fe10c7
Source noteuspto-grants-1986_12