Реакция #696700

Уравнение реакции

sodium boron hydride

sodium boron hydride

2-ethyl-4-phenyl-1-indanone

acetone

→

aimed product

Выход 99.3%

2-ethyl-1-hydroxy-4-phenylindan

Выход 99.3%

Растворители

ethanol

ethanol

Условия реакции

Обработка

1. 1
   ДругоеTo a 200-ml three-necked round flask (equipped with a stirrer tip
2. 2
   workup.ADDITIONAfter the dropwise addition
3. 3
   Другоеwas elevated to 50° C.
4. 4
   Другоеreaction for further 3.5 hours
5. 5
   ДругоеAfter the reaction
6. 6
   Температураthe mixture was cooled
7. 7
   КонцентрированиеThen, the reaction mixture was concentrated under reduced pressure
8. 8
   Экстракцияextracted with 50 ml of water and 50 ml of ether
9. 9
   ДругоеThe organic phase was separated
10. 10
    Экстракцияthe aqueous phase was extracted twice with 50 ml of ether
11. 11
    ПромывкаThe combined organic phases were washed with 100 ml of a saturated saline solution
12. 12
    Сушкаdried over anhydrous Na2SO4
13. 13
    workup.DISTILLATIONThen, the solvent was distilled off under reduced pressure

Методика

To a 200-ml three-necked round flask (equipped with a stirrer tip, a Dimroth condenser, a dropping funnel and a thermometer) were introduced 0.85 g (22.6 mmol) of sodium boron hydride and 28 ml of ethanol, and then in a nitrogen atmosphere at room temperature, a solution of 10.6 g (45.1 mmol) of 2-ethyl-4-phenyl-1-indanone in 20 ml of ethanol was dropwise added. After the dropwise addition was completed, the temperature was elevated to 50° C. to perform reaction for further 3.5 hours. After the reaction, the mixture was cooled, and acetone was dropwise added to decompose the unreacted sodium boron hydride. Then, the reaction mixture was concentrated under reduced pressure and extracted with 50 ml of water and 50 ml of ether. The organic phase was separated, and the aqueous phase was extracted twice with 50 ml of ether. The combined organic phases were washed with 100 ml of a saturated saline solution and dried over anhydrous Na2SO4. Then, the solvent was distilled off under reduced pressure to obtain 10.67 g of the aimed product (a mixture of two isomers) as a viscous, light yellow liquid (yield: 99%). The properties of the product thus obtained are described below.

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