Trimethyl Phosphate → ([1,1'-Biphenyl]-4-ylmethyl)phosphonic acid dimethyl ester

HRID 233438

Reaktionsgleichung

Reaktionsgleichung von HRID 233438
Cl[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.[CH3:15][O:16][P:17](OC)([O:19][CH3:20])=[O:18]>>[CH3:15][O:16][P:17]([CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:5][CH:4]=1)(=[O:18])[O:19][CH3:20]

Komponenten

3

Edukt 2

HCID 10541Trimethyl PhosphateHCID 154634-Phenylbenzyl chloride

Produkt 1

HCID 15359635([1,1'-Biphenyl]-4-ylmethyl)phosphonic acid dimethyl esterAusbeute 72,8 %

Versuchsvorschrift

A solution of 4-(chloromethyl)biphenyl (4.12 g, 0.020M) in trimethylphosphate (10 mL, 10.5 g, 0.085M) is heated at reflux temperature for 60 hours. The excess trimethylphosphite is removed under reduced pressure and the solid residue is chromatographed (400 g of 40-63 μm silica gel, 50 mL fractions). The sample is applied to the column in a minimum amount of EtOAc and the column is eluted with 50% EtOAc-hexane (1.2 L), 75% EtOAc-hexane (2 L), and with EtOAc. Fractions 88-136 contained the dimethyl ester (4.98 g, 0.0180M, 90%) which is crystallized from ether-pentane to give 4.09 g of title compound as white crystals, mp 70°-71° C.(fused), 76.5°-77.5° C.

Aufarbeitung

  1. temperatureat reflux temperature for 60 hours
  2. customThe excess trimethylphosphite is removed under reduced pressure
  3. customthe solid residue is chromatographed (400 g of 40-63 μm silica gel, 50 mL fractions)
  4. washthe column is eluted with 50% EtOAc-hexane (1.2 L), 75% EtOAc-hexane (2 L)
  5. customis crystallized from ether-pentane

Quellen und Nachweise

ORD-Eintrag
ord-5b23c166a0b34b7899d06d38da820797
Quelldatensatz
uspto-grants-1997_01
Patentnummer
US05593980

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