HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Hexanedione → HCID 12485849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Hexanedione | HCID 8035 | — |
| Reactant | 1-Methyl-1,3-cyclopentadiene | HCID 66775 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,4,7-trimethyl-1H-indene | HCID 11062660 | 2% |
| Product | HCID 12485849 | HCID 12485849 | 5% |
Reaction Steps
10.0 g (125 mmol) of methylcyclopentadiene were first added dropwise at 0° C. to a solution of 6.4 g (280 mmol) of sodium in 100 ml of methanol. This mixture was added dropwise at room temperature to a solution of 13.1 ml (112 mmol) of 2,5-hexanedione in 50 ml of methanol in the course of 1 hour. After the mixture had been stirred at room temperature for 4 hours, it was poured onto ice-water and acidified to pH 2. Hereafter, it was extracted with diethyl ether, dried over Na2SO4 and evaporated. The residue was chromatographed on 600 g of silica gel (long column) with hexane/methylene chloride (20:1). 0.90 g (5 %) of 3,4,7-trimethylindene (21) and 0.4 g (2%) of 2,4,7-trimethylidene (20) were obtained. For the NMR data, see Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05194619 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-ed3dc8eba88d4082a512b40449514fc3 |
| Source note | uspto-grants-1993_03 |