反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 40 °C
PROCEDURE
实验过程
To solution of 3-(4-methoxyphenyl)-2-phenylpropionic acid (4.6 g) in dry methylene chloride (26 ml) was added two drops of dry DMF. Thionylchloride (3 ml) was added and reaction mixture was stirred at 40° C. for 4 h. Solvent was evaporated under vacuum. Precipitate was dissolved to methylene chloride. Solution was cooled to 0-3° C. This solution and aluminium chloride (2.5 g) were mixed slowly over 4 hours keeping temperature under 4° C. After mixing reaction mixture was stirred at room temperature for 2 h. Reaction was quenched by pouring to dilute ice cold hydrochloric acid. Layers were separated and water solution was extracted with methylene chloride. Combined organic layers were washed with water, dried and evaporated. Crude product was triturated to give 2.9 g of 6-Methoxy-2-phenylindan-1-one. 1H-NMR (400 MHz, d6-DMSO): 7.56 (d, 1H), 7.35-7.23 (m, 4H), 7.18-7.13 (m, 3H), 4.02 (dd, 1H, J 3.9, 8.0 Hz), 3.82 (s, 3H), 3.61 (dd, 1H, J 8.0, 17.2 Hz), 3.11 (dd, 1H, J 3.9, 17.2 Hz).
WORKUP
后处理
- customreaction mixture
- customSolvent was evaporated under vacuum
- dissolutionPrecipitate was dissolved to methylene chloride
- temperatureSolution was cooled to 0-3° C
- additionThis solution and aluminium chloride (2.5 g) were mixed slowly over 4 hours
- customunder 4° C
- additionAfter mixing
- customreaction mixture
- stirringwas stirred at room temperature for 2 h
- customReaction
- customwas quenched
- additionby pouring to dilute ice cold hydrochloric acid
- customLayers were separated
- extractionwater solution was extracted with methylene chloride
- washCombined organic layers were washed with water
- customdried
- customevaporated
- customCrude product was triturated