HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78076Generated: October 28, 2026
Acetic Acid → 2-(3-Fluoro-4-(2-nitro-ethyl)-phenoxymethyl)-pyridine
https://huagongshe.com/reaction/78076
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(3-Fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)pyridine | HCID 59255227 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-Fluoro-4-(2-nitro-ethyl)-phenoxymethyl)-pyridine | HCID 59255405 | 50.8% |
Reaction Steps
To a dimethyl sulfoxide (20.0 mL) solution of 2-(3-fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)pyridine (1.20 g) described in Manufacturing Example 95-1-2 and acetic acid (1.00 mL) was added sodium borohydride (249 mg, 6.57 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 30 minutes at room temperature. 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, followed by crystallization with an ethyl acetate-heptane system and filtration to obtain the title compound (614 mg, 50.7%).
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-330b22863fd04c0fb95a52c7eacb26dc |
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| Source note | uspto-grants-2014_09 |
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