HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzophenone → Acetic acid, (4-benzoylphenoxy)-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Acetic acid, (4-benzoylphenoxy)-, ethyl ester | HCID 4686517 | — |
Reaction Steps
This molecule is an important precursor for the synthesis of the multifunctional acetophenone and benzophenone crosslinking agents disclosed in this application. The ethyl-(4-benzoyl-phenoxy)acetate was prepared by refluxing a mixture of 100.0 grams (0.51 moles) 4-hydroxybenzophenone, 85.2 grams (0.51 moles) ethyl bromoacetate and 800 ml of 2-butanone (MEK) in the presence of an excess of potassium carbonate (209 grams or 1.5 moles). After three hours, the carbonate was filtered off and the MEK removed on a rotovapor. The residue was crystallized from isopropyl alcohol to yield a white, flaky product with a sharp melting point of 82° C. The structure was confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05407971 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-4fc385aace7b45d4af3f3bd4be529699 |
| Source note | uspto-grants-1995_04 |