HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → 1-benzyloxy-3-fluoro-5-((E)-2-nitro-vinyl)-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 74892046 | HCID 74892046 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-benzyloxy-3-fluoro-5-((E)-2-nitro-vinyl)-benzene | HCID 68560309 | 68.5% |
Reaction Steps
Heat 3-benzyloxy-5-fluoro-benzaldehyde (3.75 g, 16.29 mmol), nitromethane (4.08 g, 66.79 mmol), and ammonium acetate (3.47 g, 44.96 mmol) in acetic acid (54 mL) in 125° C. oil bath under nitrogen for 4 hours. Cool to room temperature and pour into ice/water. Extract with hexanes/ethyl acetate. Dry (magnesium sulfate), filter and concentrate. Purify on 120 g silica gel eluting with 100:0 to 80:20 hexanes:ethyl acetate to give 3.05 g (68.5%) of the desired compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745438B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-56c0ab958dbe42dcbe4e9c018cf2c7b4 |
| Source note | uspto-grants-2010_06 |