HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → 2-Bromo-1-cyclopropylmethoxy-3-(2-nitro-vinyl)-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 3-Bromo-2-(cyclopropylmethoxy)benzaldehyde | HCID 59725044 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Bromo-1-cyclopropylmethoxy-3-(2-nitro-vinyl)-benzene | HCID 131735575 | — |
Reaction Steps
380 mg (1.49 mmol) 5-Bromo-6-cyclopropylmethoxy-benzaldehyde (example XIX), 239 μL (4.47 mmol) nitromethane and 115 mg (1.49 mmol) ammonium acetate in 1.2 mL AcOH are stirred at 100° C. for 2 h. The reaction mixture is cooled to r.t. and quenched by the addition of 4 mL MeOH and 0.9 mL water. After stirring at r.t. for 1 h the precipitate is filtered off and dried at 40° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340510B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-b11a8b9952fd47b09167a0a3d0bede74 |
| Source note | uspto-grants-2016_05 |