HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Cymene → 1,4-Diisopropylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Cymene | HCID 7463 | — |
| Reactant | 1,3,5-Triisopropylbenzene | HCID 12860 | — |
| Product | 1,4-Diisopropylbenzene | HCID 7486 | — |
Reaction Steps
[RuCl2 (1,3,5-triisopropylbenzene)]2 was prepared by stirring a suspension of [RuCl2 (P-cymene)]2 (3 g) in 120 mL 1,3,5-triisopropylbenzene (Aldrich, 97%) for a total of 8 hours at 190° C. under N2. The solution was cooled to room temperature and then placed in a refrigerator for 2-3 days. Solids were collected by cold filtration, washed with heptane, and dried in a vacuum oven at 70° C. A red-brown solid product was obtained (3.25 grams). 1H NMR analysis of this product was consistent with the material being 90+ % pure [RuCl2 (1,3,5-triisopropylbenzene)]2 with a small amount of unreacted [RuCl2 (p-cymene)]2. 1H NMR data for [RuCl2 (1,3,5-triisopropylbenzene)]2 (CDCl3 solvent): δ 1.3 (d, 18H), 3.1 (m, 3H), 5.2 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06156692 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-337594a37a9e4ed68ad717495a6b5b27 |
| Source note | uspto-grants-2000_12 |