HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350039Generated: October 28, 2026
Potassium Carbonate → HCID 69427244, compound
https://huagongshe.com/reaction/350039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Picolyl chloride hydrochloride | HCID 23392 | — |
| Reactant | Ethyl 3-[1-(4-hydroxybenzyl)-4-phenyl-3-pyrrolyl]propionate | HCID 23024736 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69427244 | HCID 69427244 | 69% |
Reaction Steps
A mixture of ethyl 3-[1-(4-hydroxybenzyl)-4-phenyl-3-pyrrolyl]propionate (1.31 g), 2-picolyl chloride hydrochloride (0.73 g), potassium carbonate (0.69 g) and N,N-dimethylformamide (15 ml) was stirred at room temperature overnight. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and then concentrated. The residue was subjected to silica gel column chromatography, and an oily substance was obtained from the fraction eluted with ethyl acetate-hexane (1:2, volume ratio). A mixture of the oily substance obtained, 1N aqueous sodium hydroxide solution (8 ml), tetrahydrofuran (8 ml) and ethanol (8 ml) was stirred at room temperature for 3 hours and the organic solvent was removed under reduced pressure. After adding water, the residue was neutralized by adding 1N hydrochloric acid. The colorless crystals obtained were collected by filtration to yield 3-[4-phenyl-1-[4-(2-pyridylmethoxy)benzyl]-3-pyrrolyl]propionic acid (1.06 g, yield: 69%). This was recrystallized from ethanol-water. Melting point: 109–110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07179823B1 |
|---|
| Source dataset | uspto-grants-2007_02 |
|---|
| ORD ID | ord-50f6b697f42e415d9396eb85f1813e0c |
|---|
| Source note | uspto-grants-2007_02 |
|---|