HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 4-Acetyl-4'-ethoxybiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Acetylphenyl)phenol | HCID 10330806 | — |
| Product | 4-Acetyl-4'-ethoxybiphenyl | HCID 23250433 | — |
Reaction Steps
A reaction vessel was charged with 230 g of 4-hydroxy-4'-acetylbiphenyl, 164 g of ethyl bromide, 276 g of potassium carbonate and 1.7 l of cyclohexanone. The mixture was reacted together under agitation for 3 hours at 65°-70° C. and then for 6 hours at 95°-100° C. The reaction liquid was filtered and the resultant solid matter was washed with benzene. The filtrate and the washing liquid were combined, washed with water and dried over Glauber's salt, The solvents were distilled off and the residue was recrystallized from a mixed solvent of acetone-methanol to obtain 4-ethoxy-4'-acetylbiphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05397504 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-908052fa35794ecbae223747716a08f4 |
| Source note | uspto-grants-1995_03 |