HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → 2-Methyl-5-(4-((E)-2-nitro-vinyl)-benzyl)-furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 4-(5-Methyl-furan-2-ylmethyl)-benzaldehyde | HCID 59255265 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Methyl-5-(4-((E)-2-nitro-vinyl)-benzyl)-furan | HCID 59255436 | 102.8% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a mixture of 4-(5-methyl-furan-2-ylmethyl)-benzaldehyde (96 mg, 0.48 mmol) described in Manufacturing Example 46-1-3 and acetic acid (1 mL) were added nitromethane (190 μL, 3.6 mmol) and ammonium acetate (110 mg, 1.4 mmol) at room temperature, which was stirred for 3 hours at 100° C. The reaction mixture was cooled to room temperature, and extracted by addition of water and ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over magnesium sulfate. The filtrate was concentrated under a reduced pressure to obtain the title compound (120 mg) as a crude product. This compound was used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153662B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-16e12018f7484975a1c80ab2310558a5 |
| Source note | uspto-grants-2012_04 |