HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
9,9-Dimethyl-9,10-dihydroacridine → 10-(2-Bromobenzyl)-9,9-dimethyl-9,10-dihydroacridine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 9,9-Dimethyl-9,10-dihydroacridine | HCID 22647 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Bromobenzyl bromide | HCID 76965 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 10-(2-Bromobenzyl)-9,9-dimethyl-9,10-dihydroacridine | HCID 86732664 | — |
Reaktionsschritte
9.7 g (0.243 mol) of NaH, 60% in mineral oil, are dissolved in 500 ml of dimethylformamide under protective atmosphere. 22.1 g (0.106 mol) of 9,9-dimethyl-9,10-dihydroacridine are dissolved in 500 ml of DMF and added dropwise to the reaction mixture. After 1 h at room temperature, a solution of 60.6 (242 mmol) of 2-bromobenzyl bromide in 500 ml of DMF is added dropwise. The reaction mixture is stirred at room temperature for 1 h, then poured onto ice and extracted three times with dichloromethane. The combined organic phases are dried over Na2SO4 and evaporated. The residue is extracted with hot toluene and recrystallised from toluene/n-heptane. The yield is 37 g (94%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09337430B2 |
| Quelldatensatz | uspto-grants-2016_05 |
| ORD ID | ord-98fa62764e0f4df29978c5879b2d56e5 |
| Quellennotiz | uspto-grants-2016_05 |