Farnesol → (E,E)-[[(3,7,11-Trimethyl-2,6,10-dodecatrienyl)oxy]methyl]phosphonic acid, dimethyl ester

HRID 327895

Reaktionsgleichung

Reaktionsgleichung von HRID 327895
[OH:1][CH2:2]/[CH:3]=[C:4](/[CH2:6][CH2:7]/[CH:8]=[C:9](/[CH2:11][CH2:12][CH:13]=[C:14]([CH3:16])[CH3:15])\[CH3:10])\[CH3:5].[N+](=[CH:19][P:20](=[O:25])([O:23][CH3:24])[O:21][CH3:22])=[N-]>>[CH3:5]/[C:4](/[CH2:6][CH2:7]/[CH:8]=[C:9](\[CH3:10])/[CH2:11][CH2:12][CH:13]=[C:14]([CH3:16])[CH3:15])=[CH:3]\[CH2:2][O:1][CH2:19][P:20](=[O:25])([O:23][CH3:24])[O:21][CH3:22]

Komponenten

3

Versuchsvorschrift

(E,E)-Farnesol, (5.0 mmol, 1.11 g, 1.26 ml) was stirred under argon in 10 ml of dry deoxygenated benzene (10 ml) and treated in one portion with ##STR87## (1.0 mmol, 0.442 g). The dark blue/green solution was stirred at room temperature and a solution of (1.5 g, 10.0 mmol) of dimethyl diazomethylphosphonate (prepared according to D. Seyferth et al, J. Org. Chem., 1971, vol. 36, No. 10, pages 1379 to 1386) in 20 ml of dry, deoxygenated benzene was added dropwise over 4 hours via syringe pump. After addition, the reaction mixture was stirred an additional 45 minutes. The reaction mixture was stripped of solvent and applied as a 75% ethyl acetate/Hexane solution to a flash chromatography column (50 mm diameter, 6" of silica gel) eluted with 75% ethyl acetate/hexane to afford 0.627 g, (36% yield), of the ether as a dark blue/green oil.

Aufarbeitung

  1. customof dry
  2. customdeoxygenated benzene (10 ml)
  3. additiontreated in one portion with ##STR87## (1.0 mmol, 0.442 g)
  4. custom10, pages 1379 to 1386) in 20 ml of dry
  5. customdeoxygenated benzene
  6. additionwas added dropwise over 4 hours via syringe pump
  7. additionAfter addition
  8. stirringthe reaction mixture was stirred an additional 45 minutes
  9. washeluted with 75% ethyl acetate/hexane

Quellen und Nachweise

ORD-Eintrag
ord-67e874669f144f53bde52744efee6c3b
Quelldatensatz
uspto-grants-1993_12
Patentnummer
US05273969

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