Реакция #1824147

Уравнение реакции

benzyl chloroformate

4-methoxypyridine

benzyl chloride

magnesium

→

title compound

2-Benzyl-N-benzyloxycarbonyl-2,3-dihydro-4-(1H)-pyridone

Растворители

ether

hydrochloric acid

tetrahydrofuran

tetrahydrofuran

ether

ether

Условия реакции

Обработка

1. 1
   workup.ADDITIONis then added dropwise to the reaction mixture over the course of 75 minutes
2. 2
   Температураmaintaining the temperature at -70°
3. 3
   workup.ADDITIONare added dropwise
4. 4
   Другоеthe phases are separated
5. 5
   ПромывкаThe organic phases are washed with water and brine
6. 6
   Сушкаdried over magnesium sulfate
7. 7
   Другоеevaporated to dryness
8. 8
   ДругоеThe residue is chromatographed on silica gel with hexane/ethyl acetate (3:1)

Методика

165 ml (1.16 mol) of benzyl chloroformate are added dropwise over the course of 20 minutes to a solution of 104 g (0.95 mol) of 4-methoxypyridine in 1 l of anhydrous tetrahydrofuran at -70° under argon. The thick beige suspension is then diluted with 200 ml of anhydrous tetrahydrofuran. The Grignard reagent prepared from 460 ml (1.46 mol) of a 3 molar solution of benzyl chloride in anhydrous ether and 35.5 g (1.46 mol) of magnesium turnings in 160 ml of anhydrous ether is then added dropwise to the reaction mixture over the course of 75 minutes, maintaining the temperature at -70°. After a further 10 minutes, it is allowed to warm to room temperature. It is diluted with 500 ml of ether, 900 ml of 4N hydrochloric acid are added dropwise, and the phases are separated. The organic phases are washed with water and brine, dried over magnesium sulfate and evaporated to dryness. The residue is chromatographed on silica gel with hexane/ethyl acetate (3:1). The title compound is obtained as a colourless viscous oil. TLC: hexane/ethyl acetate (1:3) Rf =0.7, IR: 1725, 1665, 1602 cm-1.

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