HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Methyl 12-Methyl-12H-dibenzo[d,g][1,3]dioxocin-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dichloroacetic Acid | HCID 6597 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethylidenebisphenol | HCID 13530914 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Methyl 12-Methyl-12H-dibenzo[d,g][1,3]dioxocin-6-carboxylate | HCID 14839712 | — |
Reaction Steps
1,1-Bis(2-hydroxyphenyl)ethane was treated with dichloroacetic acid, potassium carbonate, and potassium iodide in isopropyl alcohol as in Example 3 and the product obtained was esterified with methanol as in Example 4 to obtain 1.71 g of the title compound as a mixture of cis and trans isomers. A portion of this was recrystallized from ether to obtain a pure sample of the cis isomer of the title compound as a white solid melting at 146°-147° C. The geometry was determined by proton NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04999448 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-a3720385f4284d2ab232a24c86e9fb7d |
| Source note | uspto-grants-1991_03 |