反応式
[CH:1]1[CH:2]=[CH:3][C:4]2[C:15](=O)[C:14]3[C:9](=[C:10]([OH:18])[CH:11]=[CH:12][C:13]=3[OH:17])[C:7](=O)[C:5]=2[CH:6]=1.[BH4-].[Na+]>>[C:13]1(=[O:17])[C:14]2[C:9](=[CH:7][C:5]3[C:4]([CH:15]=2)=[CH:3][CH:2]=[CH:1][CH:6]=3)[C:10](=[O:18])[CH:11]=[CH:12]1参加物
実験手順
To a dried 100 mL-round-bottom flask equipped with stirring bar and serum cap, was added 1 g (MW 240.21; 0.0042 mol) of quinizarin (3). The compound was dried under vacuum, and then maintained under argon. Methanol (distilled over Mg), 20 mL, was added via syringe. The solution was stirred to dissolve the quinizarin and then cooled over an ice-water bath equipped with a thermometer. To it, 0.638 g (MW 38; 0.0168 mol) of sodium borohydride was added. The resulting mixture was stirred at 0° C. for 1 hour. The progress of the reaction was monitored by TLC (using hexanes: ether 1:1 as the eluant). The reaction was quenched by adding carefully 11 mL of 6 N HCl dropwise at 0° C. over a period of 10 minutes. Orange solids precipitate. The solids were collected by filtration over a fritted filter funnel, and washed several times with distilled water to remove the acid. The solid was then dried under vacuum and recrystallize from acetone-ether to give 0.83 g (95% yield) of yellow crystals, mp 204-206° C.
後処理
- customTo a dried 100 mL-round-bottom flask equipped
- customserum cap
- customThe compound was dried under vacuum
- temperaturemaintained under argon
- additionMethanol (distilled over Mg), 20 mL, was added via syringe
- stirringThe solution was stirred
- dissolutionto dissolve the quinizarin
- temperaturecooled over an ice-water bath
- customequipped with a thermometer
- stirringThe resulting mixture was stirred at 0° C. for 1 hour
- customThe reaction was quenched
- additionby adding carefully 11 mL of 6 N HCl dropwise at 0° C. over a period of 10 minutes
- filtrationThe solids were collected by filtration over a fritted filter funnel
- washwashed several times with distilled water
- customto remove the acid
- customThe solid was then dried under vacuum
- customrecrystallize from acetone-ether
出典と根拠
- ORDレコード
- ord-644b6d74dff5444ca4791790a59abda1
- 出典データセット
- uspto-grants-2004_12
- 特許番号
- US06828450B2
関連ノート
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