Реакция #586116

Уравнение реакции

4-hydroxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde

sodium hydride

2-methoxyethyl chloride

→

5,5,8,8-Tetramethyl-4-(2-methoxyethoxy)-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde

Выход 95.0%

Растворители

DMF

Условия реакции

Обработка

1. 1
   workup.STIRRINGthe medium is stirred at room temperature for 2 hours
2. 2
   Экстракцияhydrolysed and extracted with ethyl ether
3. 3
   ПромывкаThe organic phase is washed with 1N sodium hydroxide solution
4. 4
   ДругоеThe residue obtained
5. 5
   Другоеis purified by chromatography (eluent:heptane)
6. 6
   ДругоеA yellow oil is obtained (m=42.7 g; yield=95%)

Методика

34 g (148 mmol) of 4-hydroxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde are dissolved in 400 mL of anhydrous DMF. 7.2 g (178 mmol) of 60% sodium hydride are then added portionwise, and the reaction medium is stirred for 1 hour. 16.5 mL (178 mmol) of 2-methoxyethyl chloride are added dropwise, and the medium is stirred at room temperature for 2 hours and then hydrolysed and extracted with ethyl ether. The organic phase is washed with 1N sodium hydroxide solution and then three times with water. The residue obtained is purified by chromatography (eluent:heptane). A yellow oil is obtained (m=42.7 g; yield=95%).

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