Reaktion #318267

Reaktionsgleichung

vinyl magnesium bromide

Boc-cyclohexylalanine methyl ester

diisobutylaluminum hydride

toluene

toluene

→

desired product

Ausbeute 60.0%

4(S)-t-Butyloxycarbonylamino 5 cyclohexyl-3(R,S)-hydroxy-1-pentene

Ausbeute 60.0%

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe mixture was carefully quenched with methanol
2. 2
   workup.ADDITIONtreated with Rochelle salts (22 mL of saturated aqueous solution in 140 mL H2O)
3. 3
   Filtrationfiltered
4. 4
   ExtraktionAfter extracting the solids 5 times with ethyl acetate
5. 5
   Waschenthe organic phase was washed with brine
6. 6
   Sonstigedried
7. 7
   Filtrationfiltered
8. 8
   Sonstigeevaporated to an oil (10.2 g)

Vorschrift

To a stirred -78° C. solution of Boc-cyclohexylalanine methyl ester (10.2 g, 35.8 mmol) in dry toluene (60 mL) was added diisobutylaluminum hydride (34 mL of a 1.5M solution in toluene). After 30 minutes, vinyl magnesium bromide (108 mL of 1M solution in THF) was added. After stirring for 15 hours at 0° C., the mixture was carefully quenched with methanol, treated with Rochelle salts (22 mL of saturated aqueous solution in 140 mL H2O), and filtered. After extracting the solids 5 times with ethyl acetate, the extracts and filtrate were combined and the organic phase was washed with brine, dried, filtered, and evaporated to an oil (10.2 g). Chromatography on silica gel eluting with hexane/ethyl acetate mixtures provided 6.1 g (60%) of the desired product.

Quelle