HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77802Generated: October 26, 2026
Acetic Acid → 2-((4-(2-Nitroethyl)benzyl)oxy)pyridine
https://huagongshe.com/reaction/77802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (E)-2-((4-(2-Nitrovinyl)benzyl)oxy)pyridine | HCID 58076258 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-((4-(2-Nitroethyl)benzyl)oxy)pyridine | HCID 58076266 | 77.1% |
Reaction Steps
To a solution of 2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine (21.0 g, 81.9 mmol) described in Manufacturing Example 2-1-3, acetic acid (21 mL) in dimethyl sulfoxide (200 mL) was added sodium borohydride (4.96 g, 131 mmol) at room temperature while cooling appropriately. After addition of sodium borohydride, the cooling bath was removed, followed by stirring for 15 minutes at room temperature. The reaction solution was partitioned into water and ethyl acetate. The ethyl acetate layer was washed with water twice and with saturated aqueous sodium chloride once, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:3) to obtain the title compound (16.3 g, 77.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841327B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-aa3efa444f234a50a8ea449aa27832dd |
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| Source note | uspto-grants-2014_09 |
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