HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620081Generated: November 3, 2026
Potassium Carbonate → HCID 70393634, compound
https://huagongshe.com/reaction/620081
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid monomethyl ester | HCID 173322 | — |
| Reactant | HCID 54155326 | HCID 54155326 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70393634 | HCID 70393634 | — |
Reaction Steps
3.3 g (100 mmol) of 1,4-dihydro-2.6-dimethyl-4-(m-nitrophenyl)-pyridine-3,5-dicarboxylic acid 3-methyl ester, 3.5 g (10 mmol) of the bromoethoxy compound from step 1b), and 2.8 g (20 mmol) of potassium carbonate are heated at boiling in 50 ml of acetonitrile while stirring and under reflux. After approximately 20 hours, the reaction mixture is filtered and the filtrate is concentrated by evaporation under reduced pressure. The residue is dissolved in ethyl acetate and washed with water, and the organic phase is concentrated by evaporation in vacuo. Crude 1,4-dihydro-2,6-dimethyl-4-(m-nitrophenyl)-pyridine-3,5-dicarboxylic acid 3-{2-[p-(2-tertiary butoxycarbonylaminoethyl)-phenoxy]-ethyl}-ester 5-methyl ester is thus obtained and is used further in crude form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04818766 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-0c7207c7d15645d19fa99e33a43d6c77 |
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| Source note | uspto-grants-1989_04 |
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