HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087151Generated: October 29, 2026
p-Toluenesulfonic acid → HCID 13533254, compound
https://huagongshe.com/reaction/1087151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15632018 | HCID 15632018 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13533254 | HCID 13533254 | — |
Reaction Steps
3.4 Grams of methyl 3-(4-tetrahydropyranyloxy-phenyl)2(E)-propenyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate was dissolved in 50 ml of methanol, then 0.2 g of p-toluenesulfonic acid was added to the solution and the whole mixture was stirred at a room temperature for 4 hours. The reaction mixture was neutralized by adding sodium hydrogen carbonate, and methanol was removed by evaporation. The residue thus obtained was purified by means of a silica gel column chromatography (eluent: chloroform), recrystallized from benzene-ether to yield 2 g of methyl 3-(4-hydroxyphenyl)-2(E)-propenyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate as in the form of light yellow powdery substance. Melting point: 137.5°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05034395 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-74ba369a81a74f758f566f3a3e17e792 |
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| Source note | uspto-grants-1991_07 |
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