HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indene → 1H-Indene, (1-methylethylidene)bis-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indene | HCID 7219 | — |
| Reactant | 1-(1-Methylethylidene)-1H-indene | HCID 118693 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1H-Indene, (1-methylethylidene)bis- | HCID 11780671 | 13% |
Reaction Steps
18.8 cm3 (47.0 mmol) of n-butyllithium were added at 0° C. to a solution of 5.93 g (47.0 mmol) of indene (industrial, 91% pure) filtered over Al2O3. After the mixture had been stirred at room temperature for 15 minutes, the solution was slowly added dropwise to a solution of 7.40 g (47.0 mmol) of 1-isopropylideneindene. After the mixture had been stirred at room temperature for 2 hours, 50 cm3 of water were added and the mixture was extracted with diethyl ether. The yellow organic phase was dried over MgSO4. The residue which remained after the solvent had been stripped off was chromatographed on silica gel 60. 1.5 g (13%) of the product (2 isomers) could be isolated with hexane/methylene chloride (10:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063880 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-47ba5e6e961242198803e72be5e5425a |
| Source note | uspto-grants-2000_05 |