Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13102421 | HCID 13102421 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13254741 | HCID 13254741 | 95% |
Reaction Steps
196.5 g (1.34 mol) of 5-chloro-3,3-dimethylpent-1-en-4-one were added dropwise to a mixture of 184.9 g (1.34 mol) of potassium carbonate and 227.8 g (1.34 mol) of 4-hydroxybiphenyl in 1,000 ml of boiling acetone, in the course of one hour. The mixture was heated to the boil after 5 hours, allowed to cool to room temperature, and filtered off from the precipitated potassium chloride. The oil which remained after the filtrate had been concentrated was taken up in 1,000 ml of ethyl acetate. The solution was washed twice with 150 ml each of 10% strength sodium carbonate solution and water, and dried over anhydrous sodium sulphate, and the solvent was distilled off. Residual amounts of solvent were stripped off at 0.13 mbar (bath temperature: 180° C.). 357.2 (95% of theory) of 5-(biphenyl-4-yloxy)-3,3-dimethylpent-1-en-4-one of melting point 42° to 44° C. were obtained in this manner.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04960456 |
|---|
| Source dataset | uspto-grants-1990_10 |
|---|
| ORD ID | ord-dfa5290cce3e45d397292bc3e23ad926 |
|---|
| Source note | uspto-grants-1990_10 |
|---|