HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → 2,2-Difluoro-5-(2-nitro-vinyl)-benzo[1,3]dioxole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2,2-Difluoro-5-formylbenzodioxole | HCID 2736973 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2,2-Difluoro-5-(2-nitro-vinyl)-benzo[1,3]dioxole | HCID 67234079 | 56.8% |
Reaction Steps
To a solution of 2,2-difluoro-benzo[1,3]dioxole-5-carbaldehyde [5.48 g, 29.44 mmol, Intermediate (60)] and nitromethane (4.78 mL, 88.32 mmol) in acetic acid (90 mL) is added ammonium acetate (5.67 g, 73.6 mmol). The reaction mixture is heated to reflux for 5.5 hours. Acetic acid is removed in vacuo and the residue is added water (20 mL) and extracted with DCM (3×50 mL), organic layers are combined and washed with 2 N sodium hydroxide, water and brine, dried over sodium sulfate and concentrated. The solid obtained is crystallized in methanol/DCM (1:1) to yield intermediate 2,2-difluoro-5-(2-nitro-vinyl)-benzo[1,3]dioxole [3.83 g, Intermediate (61)] as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517889B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-3f567adf30e94a97ac7a768e5d4d0fc5 |
| Source note | uspto-grants-2009_04 |