HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640529Generated: October 26, 2026
Nitromethane → 2-(4-Fluoro-benzyl)-5-((E)-2-nitro-vinyl)-furan
https://huagongshe.com/reaction/640529
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 5-(4-Fluorobenzyl)furan-2-carbaldehyde | HCID 59255177 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-(4-Fluoro-benzyl)-5-((E)-2-nitro-vinyl)-furan | HCID 59255389 | 100.1% |
Reaction Steps
A mixture of 5-(4-fluoro-benzyl)-furan-2-carbaldehyde (1 g, 4.89 mmol) described in Manufacturing Example 208-1-2, nitromethane (1.32 mL, 24.5 mmol), ammonium acetate (754 mg, 9.78 mmol), and acetic acid (10 mL) was stirred for 3 hours at 100° C. This mixture was cooled to room temperature and partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (1.21 g). The title compound was used in the following reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691882B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-7f7f73e466064341b1bc32244b397a44 |
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| Source note | uspto-grants-2010_04 |
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