反応 #1702064
ord-2ccb158dc8244890a8d5a71e3e4e8d4b
反応方程式
5,6,7,8-tetrahydro-2-hydroxy-5,5,8,8-tetramethylnaphthalene
dichloromethane
aluminum chloride
propionyl chloride
→
5,6,7,8-tetrahydro-3-hydroxy-5,5,8,8-tetramethyl-2-naphthyl ethyl ketone
反応物
試薬
なし
溶媒
反応条件
温度
60°CELSIUS
詳細条件
See reaction.notes.procedure_details.
後処理
- 1抽出extracted by ethyl acetate
- 2洗浄The organic layer was washed by water
- 3乾燥a saturated sodium hydrogen carbonate aq. solution, and a saturated saline solution, dried over magnesium sulfate
- 4濃縮concentrated under reduced pressure
- 5その他The crude product was purified by silica gel column chromatography
実験手順
To 5,6,7,8-tetrahydro-2-hydroxy-5,5,8,8-tetramethylnaphthalene (204 mg, 1.00 mmol) were added anhydrous dichloromethane (1 mL), aluminum chloride (148 mg, 1.12 mmol), and propionyl chloride (101.7 mg, 1.10 mmol) followed by stirring at 60° C. for 16 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 column chromatography using hexane/ethyl acetate (20/1) as an elution solvent. The yield was 117 mg (45%).