Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isophorone | HCID 6544 | — |
| Reactant | HCID 86754651 | HCID 86754651 | — |
| Product | 3,5-Dimethylphenol | HCID 7948 | — |
Reaction Steps
Such high isophorone concentration in the crude product proves to be a great disadvantage when, in a further step, the crude 3,5-dimethylphenol is purified by means of crystallization. The isophorone passes on into the mother liquor which is rectified to obtain the 3,5-dimrethylphenol contained therein. Since isophorone and 3,5-dimethylphenol form an azeotrope, the presence of isophorone reduces the yield of distillation. In order to avoid a reduction in yield, the 3,5-dimethylphenol/isophorone fraction has to undergo special treatment. After leaching and distillation, 3,5-dimethylphenol is obtained with a purity of 96% purity. The yield of 3,5-dimethylphenol from this process fluctuates between 55 and 60% with reference to the amount of isophorone used.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05969196 |
|---|
| Source dataset | uspto-grants-1999_10 |
|---|
| ORD ID | ord-3cb34e69c8db4066af7c00502facaf3d |
|---|
| Source note | uspto-grants-1999_10 |
|---|