Reaktion #1926041

Reaktionsgleichung

lithium diisopropylamide

methyl 4-fluorophenyl-acetate

2-methylsulfanyl-pyrimidine-4-carbaldehyde

→

desired product

Ausbeute 76.0%

2-(4-fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-3-hydroxypropionic acid methyl ester

Ausbeute 76.0%

Lösungsmittel

THF

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONis added dropwise to the reaction mixture
2. 2
   Sonstigethe reaction is quenched
3. 3
   workup.ADDITIONby pouring the reaction solution into aqueous saturated NH4Cl
4. 4
   ExtraktionThe aqueous phase is extracted with ethyl acetate
5. 5
   Trocknendried (MgSO4)
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated in vacuo
8. 8
   SonstigeThe crude residue is purified over silica (33% EtOAc/hexanes)

Vorschrift

To a cold (−78° C.) solution of lithium diisopropylamide (21.4 mL of 2M solution in THF, 42.8 mmol) in THF (70 mL) is added dropwise a solution of methyl 4-fluorophenyl-acetate (6.0 g, 35.7 mmol) in THF ( 30 mL). The solution is stirred for 1 hour at −78° C. after which a solution of 2-methylsulfanyl-pyrimidine-4-carbaldehyde, 1, (6.0 g, 39.3 mmol) in THF (30 mL) is added dropwise to the reaction mixture. Stirring is continued for 45 minutes at −78° C. then the reaction is quenched by pouring the reaction solution into aqueous saturated NH4Cl. The aqueous phase is extracted with ethyl acetate. The organic phases combined, dried (MgSO4), filtered, and concentrated in vacuo. The crude residue is purified over silica (33% EtOAc/hexanes) to afford 8.7 g (76%) of the desired product as a mixture (1:1) of diastereomers. 1H NMR (300 MHz, CDCl3) δ 8.52 (dd, J=4.5, 1.5 Hz, 2H), 7.21-7.15 (m, 4H), 6.99 (t, J=9.0 Hz, 2H), 5.38 (d, J=5.4 Hz, 1H), 3.83 (d, J=5.4 Hz, 1H), 3.67 (s, 3H); ESI/MS: 276.1 (M+H).

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