HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856745Generated: October 26, 2026
Ethanol → (4-Amino-3-ethoxyphenyl)(2-pyridyl)methanol
https://huagongshe.com/reaction/856745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (3-Ethoxy-4-nitrophenyl)(2-pyridyl)methanol | HCID 22938745 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (4-Amino-3-ethoxyphenyl)(2-pyridyl)methanol | HCID 22938366 | 15.3% |
Reaction Steps
To a solution of (3-ethoxy-4-nitrophenyl)(2-pyridyl)methanol (2.5 g) in acetic acid (50 ml), reduced iron (7.5 g) was added to the mixture and the mixture was stirred overnight. Ethyl acetate and ethanol were added to the mixture, and the unnecessary substances were filtered off. The filtrate was concentrated under reduced pressure, the residue was diluted with ethyl acetate and neutralized with an aqueous solution of saturated sodium bicarbonate. The organic layer was separated and washed with saturated brine, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:2) and recrystallized from hexane-ethyl acetate, to give (4-amino-3-ethoxyphenyl)(2-pyridyl)methanol (340 mg) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262185B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-8169bdccb3c041fcaa44015a14a4478a |
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| Source note | uspto-grants-2007_08 |
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