HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 20095031, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloro-5-nitropyrimidine | HCID 82544 | — |
| Reactant | HCID 20095048 | HCID 20095048 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20095031 | HCID 20095031 | 77.4% |
Reaction Steps
1.00 g (4.06 mM) of 2-hexylindan-5-boronic acid, 0.64 g (4.04 mM) of 2-chloro-5-nitropyrimidine, 5 ml of ethanol, 6 ml of benzene, 5.6 ml of 2M-sodium carbonate aqueous solution and 0.24 g of tetrakis (triphenylphosphine) palladium (O) were mixed and heat-refluxed for 30 minutes under stirring. After the reaction, the reaction mixture was subjected to filtration under reduced pressure to obtain an insoluble matter. The insoluble matter was washed with ethyl acetate and recrystallized from acetone to obtain 1.02 g of 2-hexyl-5-(5-nitropyridine-2-yl)indan (Yield: 77.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05385692 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-15bc7e5dc48c4386bb776bd73771beb9 |
| Source note | uspto-grants-1995_01 |