HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691011Generated: October 27, 2026
Acetic Acid → 5-Methyl-2-(4-(2-nitro-ethyl)-benzyloxy)pyridine
https://huagongshe.com/reaction/1691011
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine | HCID 59255428 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Methyl-2-(4-(2-nitro-ethyl)-benzyloxy)pyridine | HCID 59255103 | 54.4% |
Reaction Steps
To a dimethyl sulfoxide (40.0 mL) solution of 5-methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine (3.50 g, 12.9 mmol) described in Manufacturing Example 44-1-3 and acetic acid (3.50 mL) was added sodium borohydride (822 mg, 20.6 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 10 minutes. Water was then added dropwise at room temperature while cooling appropriately. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:4) to obtain the title compound (1.91 g, 54.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153662B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-3e3489c56075487ca7c3e3666728d9ec |
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| Source note | uspto-grants-2012_04 |
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