HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-2-(propan-2-yl)-1H-indene → HCID 18386460, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-2-(propan-2-yl)-1H-indene | HCID 21918397 | — |
| Reactant | HCID 178424303 | HCID 178424303 | — |
| Catalyst | HCID 178418751 | HCID 178418751 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18386460 | HCID 18386460 | — |
Reaction Steps
4-Chloro-2-isopropylindene (9.8 g, 51 mmol) and NiCl2(PPh3)2 (1.8 g, 2.8 mmol) are dissolved in 150 mL of Et2O. 2-Methylphenylmagnesium bromide (51 mmol) as an Et2O solution was added to the solution and the reaction was stirred overnight at room temperature. After overnight stirring, the reaction was slowly quenched with H2O to neutralize unreacted Grignard. The solution was subsequently treated with 100 mL of 10% HCl(aq) and neutralized with saturated sodium bicarbonate aqueous solution. The organic layer was dried with magnesium sulfate and the solvent was removed by rotary evaporation. The remaining residue was loaded onto a silica gel column and eluted with hexane. Yield was 6.6 g (52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492465B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-561a8c29a44045c48f404d5f50d2a4c8 |
| Source note | uspto-grants-2002_12 |