Реакция #5353

Уравнение реакции

8-carbomethoxyoctanal

4-chlorobenzyltriphenylphosphonium chloride

water

potassium hexamethyldisilazide

→

10-(4-chlorophenyl)-dec-9-enoic acid methyl ester

Выход 13.0%

Растворители

tetrahydrofuran

tetrahydrofuran

Условия реакции

Обработка

1. 1
   workup.ADDITIONis added dropwise
2. 2
   Температураto warm to room temperature
3. 3
   workup.STIRRINGstirred for 2 days
4. 4
   Экстракцияextracting three times with diethyl ether
5. 5
   Промывкаwashed with brine
6. 6
   Сушкаdried over Na2SO4
7. 7
   Фильтрацияfiltered
8. 8
   Концентрированиеconcentrated in vacuo
9. 9
   Другоеto give a yellow solid
10. 10
    ФильтрацияPad filtration through flash silica gel eluting with 10% ethyl acetate/hexane
11. 11
    Другоеgives a yellow oil
12. 12
    Концентрированиеafter concentration in vacuo
13. 13
    ПромывкаFlash chromatography on a 60 mm×150 mm silica column eluting with 5% ethyl acetate/hexane

Методика

To a solution of 18.2 g (43 mmol) of 4-chlorobenzyltriphenylphosphonium chloride in 200 mL of dry tetrahydrofuran at -78° C. is added dropwise, 30.7 mL (43 mmol) of a 1.4M solution of potassium hexamethyldisilazide in tetrahydrofuran. This is allowed to stir for 1 hour when 8.0 g (43 mmol) of 8-carbomethoxyoctanal is added dropwise. The solution is stirred at -78° C. for 2 hours, allowed to warm to room temperature, and stirred for 2 days. The reaction is worked up by adding water and extracting three times with diethyl ether. The ether extracts are combined, washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give a yellow solid. Pad filtration through flash silica gel eluting with 10% ethyl acetate/hexane, gives a yellow oil after concentration in vacuo. Flash chromatography on a 60 mm×150 mm silica column eluting with 5% ethyl acetate/hexane gives 1.62 g (13%) of 10-(4-chlorophenyl)-dec-9-enoic acid methyl ester as a mixture of E and Z isomers.

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