HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Diisopropylnaphthalene → Naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Diisopropylnaphthalene | HCID 32241 | — |
| Reactant | 1,2-Diisopropylnaphthalene | HCID 3023651 | — |
| Solvent | 2,7-Diisopropylnaphthalene | HCID 94505 | — |
| Product | Naphthalene | HCID 931 | — |
Reaction Steps
Naphthalene (80 g) and the catalyst from example 1 (4 g or 5% by weight on the naphthalene) are contacted with propylene at a temperature of 220° C. with an added pressure of propylene of 0.8×105Pa for 3 hours in a 300 ml Parr pressure autoclave operated under agitation. Analysis of the reaction mixture by gas chromatography gives a conversion of 89.0%, a yield in the 2,6-diisopropyl naphthalene of 34.4% and a yield in 2,7-diisopropyl naphthalene of 11.8%. The sum of the diisopropyl naphthalene represents 51.7% of the conversion. The selectivity to the 2,6-diisopropyl naphthalene is 38.7% and the selectivity to the 2,7-diisopropyl naphthalene is 13.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05233111 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-be31893a07f048138f6042a33214b228 |
| Source note | uspto-grants-1993_08 |