HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dimethylnaphthalene → 2,7-Dimethylnaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dimethylnaphthalene | HCID 11387 | — |
| Reactant | 2,7-Dimethylnaphthalene | HCID 11396 | — |
| Solvent | P-Xylene | HCID 7809 | — |
| Product | 2,7-Dimethylnaphthalene | HCID 11396 | — |
| Product | 2,6-Dmn 2,7-dmn | HCID 131715796 | — |
Reaction Steps
An agitation vessel of the same type as used in the crystallizing steps of Example 1 was charged with 152.2 g of a solution consisting of 2,6-DMN, 2,7-DMN and paraxylene at a weight ratio of 9:9:82 and the charged solution was cooled from 19.5° C. to 7.0° C. over a period of 72 minutes. The change in the composition of the liquid phase in the solution with time was analyzed and it was found that 2,6 -DMN and 2,7-DMN formed a eutectic mixture at a 2,6-DMN/2,7-DMN ratio of 0.59.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791235 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-861ee37f3c3744f68d5e2072ebea0271 |
| Source note | uspto-grants-1988_12 |