Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Propionic anhydride | HCID 31263 | — |
| Reactant | 3-Hexanone, 5-methyl-5-phenyl- | HCID 78639 | — |
| Reactant | HCID 178418740 | HCID 178418740 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Methyl-2-phenylhexenol | HCID 54091258 | — |
Reaction Steps
A process for preparing 2-methyl-2-phenyl-4-hexanone having the structure: ##STR47## comprising the step of intimately admixing propionic anhydride having the structure: ##STR48## with neophymagnesium chloride having the structure: ##STR49## in the presence of an inert solvent selected from the group consisting of diethylether, toluene and tetrahydrufuran, the reaction taking place in the presence of or in the absence of a cuprous chloride catalyst; the mole ratio of propionic anhydride:neophylmagnesium chloride being from 0.5:1 up to about 2:1; the temperature of reaction being from -10° C. up to 0° C.; the concentration of propionic anhydride in solvent being from about 1 up to about 5 moles of propionic anhydride per liter of solvent; the time of addition of one reactant to the other varying from 0.5 hours up to 4 hours and the time of aging of the reaction mass being from 0.5 up to 4 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04450296 |
|---|
| Source dataset | uspto-grants-1984_05 |
|---|
| ORD ID | ord-99778318ba0c486382fd533fe8c46591 |
|---|
| Source note | uspto-grants-1984_05 |
|---|