Реакция #2273688

Уравнение реакции

diisopropylamine

n-butyllithium

benzyl bromide

methyl (S)-3-hydroxybutyrate

→

title compound

Выход 61.0%

Methyl (2S,3S)-2-Benzyl-3-Hydroxybutyrate

Выход 61.0%

Растворители

tetrahydrofuran

hexamethylphosphoramide

hexane ethyl acetate

Условия реакции

Обработка

1. 1
   workup.ADDITIONwas added
2. 2
   workup.ADDITIONas above was added
3. 3
   workup.STIRRINGAfter the mixture was stirred for 0.5 hour
4. 4
   workup.ADDITIONwas added
5. 5
   Другоеdropwise at −10° C.
6. 6
   workup.ADDITIONAfter the addition
7. 7
   Температураthe temperature was heated up to 0° C.
8. 8
   workup.STIRRINGthe mixture was stirred for 15 min
9. 9
   Экстракцияwas extracted with ethyl acetate
10. 10
    КонцентрированиеThe ethyl acetate layer was concentrated
11. 11
    Другоеto give 3.90 g of a crude product

Методика

Subsequently, in a 50 ml flask were charged 3.3 g (30.0 mmol) of diisopropylamine and 10 ml of tetrahydrofuran, and 16.6 ml (24.9 mmol) of n-butyllithium 1.5M hexane solution was added thereto dropwise on an ice bath in a nitrogen stream. The mixture was then stirred for 1 hour at that temperature. The reaction mixture was further cooled to −40° C., and 1.40 g (11.9 mmol) of methyl (S)-3-hydroxybutyrate prepared as above was added thereto dropwise. After the mixture was stirred for 0.5 hour, 3.00 g (17.5 mmol) of benzyl bromide dissolved in 6 ml of hexamethylphosphoramide was added thereto dropwise at −10° C. or lower temperature. After the addition, the temperature was heated up to 0° C., and the mixture was stirred for 15 min. The resulting mixture was then poured into an ice water, and was extracted with ethyl acetate. The ethyl acetate layer was concentrated to give 3.90 g of a crude product. The crude product was subjected to column chromatography (hexane/ethyl acetate=4/1 by volume) to obtain 1.50 g (61%) of the title compound (anti/syn=98/2).

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