反应 #1356

反应方程式

2-ethyl-1-hydroxy-4-(9-phenanthryl)indane

triethylamine

sodium bicarbonate

methansulfonyl chloride

→

desired product

收率 83.0%

2-ethyl-4-(9-phenathryl)indene

收率 83.0%

溶剂

methylene chloride

methylene chloride

反应条件

后处理

1. 1
   其他A 300-ml three-necked round flask equipped with a stirring bar
2. 2
   workup.ADDITIONTo the mixture was gradually dropwise added a solution
3. 3
   workup.ADDITIONAfter the addition
4. 4
   其他was elevated to room temperature
5. 5
   其他The organic phase was separated
6. 6
   萃取the aqueous phase was extracted with 50 ml of methylene chloride two times
7. 7
   洗涤The combined organic phase was washed with water
8. 8
   干燥by drying over anhydrous Na2SO4
9. 9
   其他The solvent was evaporated under reduced pressure
10. 10
    其他The residue was chromatographed on silica gel (eluting with hexane, and hexane/ethyl acetate (100/3 parts by volume))

实验过程

A 300-ml three-necked round flask equipped with a stirring bar, a Dimroth condenser, a dropping funnel and a thermometer was charged with 12.3 g (36.3 mmol) of 2-ethyl-1-hydroxy-4-(9-phenanthryl)indane, 19.7 ml (142 mmol) of triethylamine and 61.5 ml of methylene chloride. To the mixture was gradually dropwise added a solution containing 3.3 ml (42.6 mmol) of methansulfonyl chloride dissolved in 5 ml of methylene chloride under a nitrogen atmosphere at 0° C. After the addition was completed, the temperature was elevated to room temperature, and the reaction mixture was stirred for additional 4 hours. To the reaction mixture was added 80 ml of a saturated aqueous solution of sodium bicarbonate. The organic phase was separated, and the aqueous phase was extracted with 50 ml of methylene chloride two times. The combined organic phase was washed with water, and then a saturated aqueous solution of sodium chloride, followed by drying over anhydrous Na2SO4. The solvent was evaporated under reduced pressure. The residue was chromatographed on silica gel (eluting with hexane, and hexane/ethyl acetate (100/3 parts by volume)) to give 9.61 g of the desired product (mixture of two isomers) as a pasty pale yellow-green liquid (yield: 83%).

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