HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylaldehyde → HCID 10899688, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromocyclohexene | HCID 137057 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 10899688 | HCID 10899688 | 92.9% |
Reaction Steps
In a 10-liter reactor there were introduced 633.4 g (5.19 moles) of salicylaldehyde, 5 liters of acetone and 717.3 g of potassium carbonate, and the mixture was left with stirring at room temperature. After precipitation of the phenate, 836 g (5.19 moles) of 3-bromocyclohexene were rapidly added dropwise, and the mixture was brought to reflux for 21/2 hours. After removal of the inorganic salts by filtration, and evaporation of the solvent, the residue was taken up in ethyl ether, washed with 10% caustic soda and then water, and the ether phase was then dried over Na2SO4. After filtration and elimination of the ether, there were obtained 975 g of 3-(2-formylphenoxy)cyclohexene, which was used directly in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04631277 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-85daf6bea9884c8197cecc290f059289 |
| Source note | uspto-grants-1986_12 |