HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116498Generated: October 31, 2026
Sodium Bicarbonate → HCID 23103617, compound
https://huagongshe.com/reaction/2116498
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 69220512 | HCID 69220512 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | HCID 23103617 | HCID 23103617 | 41.3% |
Reaction Steps
To a solution of 4-ethylphenyl-[3-[2-(triethylsilyl)ethoxymethoxy]]pyridin-2-yl-methanol (2.35 g, 6.54 mmol) in THF-water (25:1; 60 mL), p-toluenesulfonic acid monohydrate (2.8 g, 16.4 mmol) was added and stirred at room temperature for 20 hours and at 40° C. for 4 hours. After cooling the reaction mixture to room temperature, saturated sodium bicarbonate solution (100 mL) was added and the resulting mixture was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to give 4-ethylphenyl-3-hydroxypyridin-2-yl-methanol (0.62 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439232B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-092eb62a49484917bc40e88e61630e6d |
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| Source note | uspto-grants-2008_10 |
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