Reaktion #1444601

Reaktionsgleichung

(2S)-2-methyl-4-pentenal

1,1-diisopropoxy-2,2,-dimethyl-3-butanone

lithium diisopropylamide

water

→

(5R,6S)-1,1-diisopropoxy-5-hydroxy-2,2,6-trimethyl-8-nonen-3-one

Lösungsmittel

ether

ether

ether

ether

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwarmed to −40° C.
2. 2
   workup.STIRRINGstirred for 30 minutes
3. 3
   Sonstigerecooled to −78° C
4. 4
   workup.STIRRINGthe reaction is stirred for an additional 30 minutes at −78° C.
5. 5
   Temperaturwarmed to −30° C.
6. 6
   workup.WAITkept for 45 minutes
7. 7
   Sonstigerecooled to −78° C
8. 8
   workup.STIRRINGthe mixture is stirred for 2 hours at −78° C
9. 9
   workup.STIRRINGthe mixture is stirred for 1 hour
10. 10
    Filtrationfiltered through Celite
11. 11
    WaschenThe filtrate is washed with sat. aq. NaCl
12. 12
    Extraktionthe brine layer is back extracted with ether
13. 13
    Trocknendried with Na2SO4
14. 14
    Filtrationfiltered
15. 15
    Sonstigeevaporated
16. 16
    SonstigeThe product is purified by chromatography on SiO2

Vorschrift

A solution of 1,1-diisopropoxy-2,2,-dimethyl-3-butanone (3.08 g) in 15 mL of ether is added slowly to a solution of lithium diisopropylamide (15.7 mmol) in 20 mL of ether cooled to −78° C., the mixture is stirred for 30 minutes, warmed to −40° C. and stirred for 30 minutes, then recooled to −78° C. A solution of bis(1,2:5,6-di-O-isopropylidene-α-D-glucofuranos-3-O-yl)cyclopentadienyltitanium chloride (17.4 mmol) in 180 mL of ether is added dropwise over 40 minutes, and the reaction is stirred for an additional 30 minutes at −78° C., warmed to −30° C. and kept for 45 minutes, then recooled to −78° C. A solution of (2S)-2-methyl-4-pentenal (16.36 mmol) in 30 mL of ether is added over 10 minutes and the mixture is stirred for 2 hours at −78° C. A 5 M solution of water in THF (28 mL) is added, the mixture is stirred for 1 hour and then filtered through Celite. The filtrate is washed with sat. aq. NaCl, and the brine layer is back extracted with ether. The organic phases are combined, dried with Na2SO4, filtered, and evaporated. The product is purified by chromatography on SiO2.

Quelle