反応式
C([O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[C:7]([CH3:15])[CH:6]=1)(=O)C>[OH-].[K+]>[CH3:15][C:7]1[CH:6]=[C:5]([OH:4])[C:14]2[C:9]([CH:8]=1)=[CH:10][CH:11]=[CH:12][CH:13]=2参加物
3
実験手順
Crude 1-acetoxy-3-methylnaphthalene (84 g, 0.42 mole) was boiled with 10% ethanolic potassium hydroxide (300 cm3) for 3 hours. Ethanol was distilled off and the residue dissolved in water and extracted with toluene to remove neutral products. The aqueous alkaline solution was carefully acidified with dilute hydrochloric acid and the liberated 3-methyl-l-naphthol extracted with ether. The ether extract was washed with water, dried and filtered. Ether solvent was removed leaving 3-methyl-l-naphthol (18.4 g) as clear colorless crystals.
後処理
- distillationEthanol was distilled off
- dissolutionthe residue dissolved in water
- extractionextracted with toluene
- customto remove neutral products
- extractionthe liberated 3-methyl-l-naphthol extracted with ether
- extractionThe ether extract
- washwas washed with water
- customdried
- filtrationfiltered
- customEther solvent was removed
出典と根拠
- ORDレコード
- ord-12990e0e8b8d420b9995ac40ed251615
- 出典データセット
- uspto-grants-1993_04
- 特許番号
- US05200116
関連ノート
読み込み中…