HuagongsheHuagongshe Chemistry Print Report · For research reference only
Gamma-Butyrolactone → 1(2H)-Naphthalenone, 3,4-dihydro-5,8-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Gamma-Butyrolactone | HCID 7302 | — |
| Reactant | P-Xylene | HCID 7809 | — |
| Product | 1(2H)-Naphthalenone, 3,4-dihydro-5,8-dimethyl- | HCID 99334 | 23.2% |
Reaction Steps
Using the same reactor as in Example 1, 3.20 g of the 10 wt % HSiW/SiO2 catalyst (0.097 mmol-HSiW) as the catalyst produced in Example 1, 100 ml of p-xylene (799 mmol) and 1 ml of γ-butyrolactone (14.8 mmol) were reacted at 196° C. for 3 hours to obtain 5,8-dimethyltetralone (yield based on γ-butyrolactone: 30.4%). After removing the supernatant by filtration, 100 ml of p-xylene (799 mmol) and 1 ml of γ-butyrolactone (14.8 mmol) as raw materials were charged again and then reacted at 196° C. for 3 hours. As a result, 5,8-dimethyltetralone (yield based on γ-butyrolactone: 23.2%) was obtained. The catalyst could be reused.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115782B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-691162b308db49589b4632c5ba005a72 |
| Source note | uspto-grants-2006_10 |