Reaktion #1702069
ord-6176243e874449c1aced6cbc468c3be3
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Extraktionextracted by ethyl acetate
- 2WaschenThe organic layer was washed by water
- 3Trocknena saturated sodium hydrogen carbonate aq. solution, and a saturated saline solution, dried over magnesium sulfate
- 4Einengenconcentrated under reduced pressure
- 5SonstigeThe crude product was purified by silica gel chromatography
Vorschrift
The synthesis process is as set forth in the chemical reaction formula below. To 5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene (188 mg, 1.00 mmol) were added anhydrous dichloromethane (1 mL), aluminum chloride (140 mg, 1.05 mmol), and isobutyryl chloride (112 mg, 1.05 mmol) followed by stirring at room temperature for 3 hours. The reaction solution was poured into cold water and extracted by ethyl acetate. The organic layer was washed by water, a saturated sodium hydrogen carbonate aq. solution, and a saturated saline solution, dried over magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography using hexane/ethyl acetate (20/1) as an elution solvent. The yield was 97.4 mg (38%).