HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1644211Erstellt: 24. Oktober 2026
Cesium carbonate → 2-bromo-6-(6-tert-butyl-1-oxophthalazin-2(1H)-yl)benzaldehyde
https://huagongshe.com/de/reaction/1644211
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | 4,7-Dimethoxy-1,10-phenanthroline | HCID 10462298 | — |
| Edukt | 2,6-Dibromobenzaldehyde | HCID 12648641 | — |
| Edukt | 6-(tert-butyl)phthalazin-1(2H)-one | HCID 57633933 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-bromo-6-(6-tert-butyl-1-oxophthalazin-2(1H)-yl)benzaldehyde | HCID 58016185 | 69,1% |
Reaktionsschritte
5.90 g (22.4 mmol) of 2,6-dibromobenzaldehyde, 1.80 g (8.90 mmol) of 6-tert-butyl-2H-phthalazin-1-one, 6.02 g (18.5 mmol) of cesium carbonate, 179 mg (0.940 mmol) of copper(I) iodide, and 428 mg (1.87 mmol) of 4,7-dimethoxy-1,10-phenanthroline were weighed into a 100 mL reaction flask fitted with a stir bar and septum cap. Added 50 mL of anhydrous dioxane. Purged the reaction mixture with nitrogen for 15 min. Stirred at 100° for 18 h. Partitioned the reaction mixture between 200 mL of 10% MeOH/CH2Cl2 and 200 mL of water. Separated phases and extracted the aqueous phase with 2×100 mL of 10% MeOH/CH2Cl2. The combined organic extracts were washed with 200 mL of brine, dried over Na2SO4, and the solvent was removed on rotavap. Purified the crude by flash chromatography on silica gel to obtain 2.37 g of the title compound as an off-white solid. MS (ESI) doublet 385, 387 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08124604B2 |
|---|
| Quelldatensatz | uspto-grants-2012_02 |
|---|
| ORD ID | ord-06397d36b03640b9bc2d8b9d7efb6adb |
|---|
| Quellennotiz | uspto-grants-2012_02 |
|---|