HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropyl iodide → 4-(Diethylamino)-2-(1-methylethoxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Diethylamino)-2-hydroxybenzaldehyde | HCID 87293 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Diethylamino)-2-(1-methylethoxy)benzaldehyde | HCID 86639492 | 91.3% |
Reaction Steps
To a suspension of 4-diethylamino-2-hydroxybenzaldehyde (300 mg, 1.55 mmol), potassium carbonate (428 mg, 3.10 mmol), and cesium carbonate (50 mg, 0.15 mmol) in 1.6 mL of dry N,N-dimethylformamide was added 2-iodopropane (0.47 mL, 4.7 mmol) at room temperature. After being stirred at the same temperature for 7 h, the reaction mixture was filtered to remove inorganic salts. The filtrate was diluted with diethyl ether, and the solution was washed with water, saturated NaHCO3 aqueous solution, brine, and dried over MgSO4. After filtration, the filtrate was concentrated in vacuo, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=90/10 to 75/25) to obtain the title compound as a colorless oil (333 mg, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08962674B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-b180625d7c5f447e97dd38125ea53c5f |
| Source note | uspto-grants-2015_02 |