HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614669Generated: November 1, 2026
1,2-Dimethoxyethane → HCID 19772294, compound
https://huagongshe.com/reaction/1614669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Diethyl Succinate | HCID 31249 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 19772209 | HCID 19772209 | — |
| Product | HCID 19772294 | HCID 19772294 | — |
Reaction Steps
A solution of 1.25 g of 2-[(E)-2-(3-aminophenyl)ethenyl]-6-[4-(4-methylphenyl)butoxy]methylpyridine, 1.05 g of anhydrous diethyl succinate, 0.6 g of sodium acetate and 10 ml of dimethoxyethane was stirred under reflux for 5 hours. After completion of the reaction, the solvent was distilled off and to the residue was added water. After extracting with ethyl acetate, the organic layer was dried over anhydrous magnesium sulfate and the solvent was distilled off. To the residue was added isopropyl ether, the precipitated crystals were collected by filtration and recrystallized from ethanol to give 0.63 g of 2-[(E)-2-(3-(3-carboxy-3-ethylvalerylamino)phenyl)ethenyl]-6-[4-(4-methylphenyl)butoxy]methylpyridine, melting at 141°-142° C. as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05198452 |
|---|
| Source dataset | uspto-grants-1993_03 |
|---|
| ORD ID | ord-d147dd7488a54e9eb6515a2917e0deb5 |
|---|
| Source note | uspto-grants-1993_03 |
|---|