Reaktion #2475556

ord-17cf7b6f787c4d3f9cfa940d40944993

Reaktionsgleichung

O=C(O)C(F)(F)F
trifluoroacetic acid
C[O-].[Na+]
sodium methoxide
COP(=O)([O-])OC
dimethyl phosphate
COc1cc(C=O)cc(OC)c1OC
3,4,5-trimethoxybenzaldehyde
COc1cc(C(O)P(=O)(OC)OC)cc(OC)c1OC
1
Ausbeute 88.0%
COc1cc(C(O)P(=O)(OC)OC)cc(OC)c1OC
[Hydroxy-(3,4,5-trimethoxy-phenyl)-methyl]-phosphonic Acid Dimethyl Ester
Ausbeute 88.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA round-bottom flask equipped with thermometer, condenser and gas inlet
  2. 2
    TemperaturA resulted solution was heated at 50° C. for 1 hour
  3. 3
    Temperaturcooled down to r.t.
  4. 4
    EinengenThe mixture was concentrated under reduced pressure
  5. 5
    workup.DISSOLUTIONthe residue dissolved in EtOAc (300 mL)
  6. 6
    Waschenwashed once with 18% brine
  7. 7
    Trocknenonce with saturated brine, dried over sodium sulfate
  8. 8
    EinengenThe filtered solution was concentrated until precipitation
  9. 9
    workup.ADDITIONTo the resulted suspension 1:1 mixture of t-butylmethyl ether and heptane
  10. 10
    workup.ADDITIONwas added (50 mL)
  11. 11
    FiltrationSolid was filtered out
  12. 12
    Waschenwashed with two portions (20 mL) of the same solvent mixture
  13. 13
    Sonstigevacuum-dried

Vorschrift

A round-bottom flask equipped with thermometer, condenser and gas inlet was charged with methanol (150 mL) and sodium methoxide (1.074 g, 20 mmol) and cooled to 0° C. under nitrogen protection. To a stirred solution were added subsequently dimethyl phosphate (19.52 g, 0.177 mol) and 3,4,5-trimethoxybenzaldehyde (30 g, 0.153 mol). A resulted solution was heated at 50° C. for 1 hour, cooled down to r.t. and treated with trifluoroacetic acid (4.6 ml). The mixture was concentrated under reduced pressure, the residue dissolved in EtOAc (300 mL), washed once with 18% brine, then once with saturated brine, dried over sodium sulfate. The filtered solution was concentrated until precipitation started. To the resulted suspension 1:1 mixture of t-butylmethyl ether and heptane was added (50 mL). Solid was filtered out, washed with two portions (20 mL) of the same solvent mixture and vacuum-dried to give 41.2 g (88%) of 1, LC purity 99.4% (AUC), m.p. 103-104° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08269017B2uspto-grants-2012_09