HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Bromo-3-fluorobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Bromo-3-fluorobenzylidene diacetate | HCID 53633065 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Bromo-3-fluorobenzaldehyde | HCID 2783411 | — |
Reaction Steps
A mixture of 4-bromo-3-fluorobenzylidene diacetate (15 g), ethanol (41 ml), water (41 ml) and concentrated sulphuric acid (4 ml) was heated to reflux for 3 hours. After cooling, ether (300 ml) was added and the aqueous layer separated. The organic phase was washed with saturated sodium carbonate and brine before drying over anhydrous magnesium sulphate and evaporation in vacuo. 4-Bromo-3-fluorobenzaldehyde was obtained as a solid (7.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05061726 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-b2bf3b052c1e4a8cba5a34f25d501af9 |
| Source note | uspto-grants-1991_10 |