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Diethyl Ether → 3-Methyl-2-oxohept-5-ynylphosphonic acid dimethyl ester

HRID 1632239
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1632239
[CH3:1][P:2]([O:6][CH3:7])(=[O:5])[O:3][CH3:4].[CH2:8]([Li])[CH2:9][CH2:10][CH3:11].C[CH2:14][O:15]CC.O1CC[CH2:20][CH2:19]1>>[CH3:11][CH:10]([CH2:9][C:8]#[C:19][CH3:20])[C:14](=[O:15])[CH2:1][P:2]([O:6][CH3:7])(=[O:5])[O:3][CH3:4]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 3283Diethyl EtherHCID 8028Tetrahydrofuran2×HCID 12958Dimethyl methylphosphonateHCID 178418339Butyllithium

Produkt 1

HCID 110426053-Methyl-2-oxohept-5-ynylphosphonic acid dimethyl ester

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

Next, to a solution of 18 g of dimethyl methanephosphonate in 294 ml of anhydrous tetrahydrofuran was added at -78° C. 86 ml of n-butyl lithium (1.5N), and the mixture was stirred for 20 mins. To the thus prepared reaction mixture was added a solution of 10.4 g of the above-mentioned ester in 20 ml of anhydrous tetrahydrofuran. Then, the mixture was stirred for 15 mins at -78° C. and for 1 hour at room temperature, and 300 ml of ether was added. The solution was washed with 150 ml of aqueous saturated solution of oxalic acid, 150 ml of water and 50 ml of aqueous saturated solution of sodium chloride and condensed. The residue was distilled under a reduced pressure to give 14.7 g of dimethyl 3-methyl-2-oxo-hept-5-yne-phosphonate (138° to 142° C./0.62 mmHg).

Aufarbeitung

  1. customTo the thus prepared reaction mixture
  2. washThe solution was washed with 150 ml of aqueous saturated solution of oxalic acid, 150 ml of water and 50 ml of aqueous saturated solution of sodium chloride and condensed
  3. distillationThe residue was distilled under a reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-0ab3f5f6ed3f4eb79df050ca54c48c45
Quelldatensatz
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04474802

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