Reacción #1361

Ecuación de reacción

water

2-i-butyl-1-hydroxy-4-(1-naphthyl)indene

triethylamine

methanesulfonyl chloride

→

desired product

Rendimiento 93.0%

2-i-butyl-4-(1-naphthyl)indene

Rendimiento 93.0%

Disolventes

methylene chloride

methylene chloride

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroA 200-ml three-necked round flask equipped with a stirring bar
2. 2
   workup.ADDITIONTo the mixture was added dropwise a solution
3. 3
   Temperaturawhile cooling with ice bath
4. 4
   workup.ADDITIONAfter the addition
5. 5
   Otrowas elevated to room temperature
6. 6
   OtroThereafter, the organic phase was separated
7. 7
   Extracciónthe aqueous phase was extracted with 50 ml of methylene chloride
8. 8
   Lavadowashed with a saturated NaCl aq.
9. 9
   Secadoby dried over anhydrous Na2SO4
10. 10
    OtroThe solvent was evaporated under reduced pressure
11. 11
    OtroThe residue was separated
12. 12
    Otropurified with silica gel chromatography (eluting with hexane/ethyl acetate (20/1 parts by volume))

Procedimiento

A 200-ml three-necked round flask equipped with a stirring bar, a Dimroth condenser, a dropping funnel and a thermometer was charged with 4.54 g (14.4 mmol) of 2-i-butyl-1-hydroxy-4-(1-naphthyl)indene, 5.13 g (50.8 mmol) of triethylamine, 0.10 g (0.82 mmol) of 4-dimethylaminopyridine and 57.7 ml of methylene chloride. To the mixture was added dropwise a solution containing 3.87 ml (33.8 mmol) of methanesulfonyl chloride dissolved in 7.7 ml of methylene chloride under a nitrogen atmosphere while cooling with ice bath. After the addition was completed, the temperature was elevated to room temperature and the mixture was further stirred for 3 hours. The reaction mixture was poured onto 100 ml of water. Thereafter, the organic phase was separated, and the aqueous phase was extracted with 50 ml of methylene chloride. The extracted organic phases were combined and washed with a saturated NaCl aq., followed by dried over anhydrous Na2SO4. The solvent was evaporated under reduced pressure. The residue was separated and purified with silica gel chromatography (eluting with hexane/ethyl acetate (20/1 parts by volume)) to obtain 3.98 g of the desired product (mixture of two isomers) as a pale yellow pasty liquid (yield: 93%).

Fuente