HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77965Generated: October 28, 2026
Acetic Acid → 1-(2-Nitro-ethyl)-3-phenoxy-benzene
https://huagongshe.com/reaction/77965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(2-Nitroethenyl)-3-phenoxybenzene | HCID 5702505 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Nitro-ethyl)-3-phenoxy-benzene | HCID 59255170 | 68.1% |
Reaction Steps
To a dimethyl sulfoxide (30.0 mL) solution of 1-((E)-2-nitro-vinyl)-3-phenoxy-benzene (3.60 g, 14.9 mmol) described in Manufacturing Example 64-1-1 and acetic acid (3.00 mL) was added sodium borohydride (902 mg, 23.8 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 3 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 reduce pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:5) to obtain the title compound (2.47 g, 68.1%).
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-1a2d720998ef4415a6434f30c7b3a947 |
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| Source note | uspto-grants-2014_09 |
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