HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 4-(1-Fluorocyclopropyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | HCID 68703601 | HCID 68703601 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(1-Fluorocyclopropyl)benzoic acid | HCID 66599234 | 46% |
Reaction Steps
Oxygen was slowly bubbled at 100° C. through a solution of 1-(1-fluoro-cyclopropyl)-4-methyl-benzene (470 mg, 3.13 mmol), cobalt(II)acetate tetrahydrate (117 mg, 0.46 mmol), and acetaldehyde (0.18 mL, 3.1 mmol) in acetic acid (30 mL) over 16 h. After cooling, the reaction mixture was evaporated and the residue triturated in water. The precipitate was collected by filtration to produce the title compound (257 mg, 46%). Light green solid, MS (EI) 180.1 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678818B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-61b79f41742d4eef8ce098b7f76c38d3 |
| Source note | uspto-grants-2010_03 |