HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → Diphenyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Product | Diphenyl Ether | HCID 7583 | — |
Reaction Steps
Method G illustrates still another means for obtaining intermediate XIII. In this method, substituted propriolate ester XVI is reacted with amidoxime XVII in a suitable solvent (e.g., alcohol, acetonitrile, THF, dimethylsulfoxide (DMSO), acetone, DMF) at about 0° C. to the reflux temperature of the solvent for about 1-48 hours to obtain olefin XVIII wherein when R1 =H, a mixture of cis and trans isomers is obtained, and when R1 =alkyl or aryl, a mixture of E and Z isomers is obtained. Further treatment of olefin XVIII in solvents such as DMF, DMSO, diphenylether, xylene, and the like, at 0° C. to the reflux temperature of the solvent for about 1-48 hours affords intermediate XIII, preferably for 1 hour in diphenylether at 180°-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04853383 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-a2cfd35f00514594ac190a5ec1c78e50 |
| Source note | uspto-grants-1989_08 |