Tri-o-tolylphosphine → diisopropyl (2S,3R)-2-hydroxy-3-{(2E)-3-[4-(trifluoromethoxy)phenyl]-2-propenyl}butanedioate

HRID 1677789Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1677789
[CH2:1]([C@H:4]([C@H:11]([OH:18])[C:12]([O:14][CH:15]([CH3:17])[CH3:16])=[O:13])[C:5]([O:7][CH:8]([CH3:10])[CH3:9])=[O:6])[CH:2]=[CH2:3].Br[C:20]1[CH:25]=[CH:24][C:23]([O:26][C:27]([F:30])([F:29])[F:28])=[CH:22][CH:21]=1.C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C>CC#N.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[OH:18][C@@H:11]([C@@H:4]([CH2:1]/[CH:2]=[CH:3]/[C:20]1[CH:21]=[CH:22][C:23]([O:26][C:27]([F:28])([F:29])[F:30])=[CH:24][CH:25]=1)[C:5]([O:7][CH:8]([CH3:10])[CH3:9])=[O:6])[C:12]([O:14][CH:15]([CH3:17])[CH3:16])=[O:13]

Komponenten

6

Edukt 3

HCID 80271Tri-o-tolylphosphineHCID 5210081-Bromo-4-(trifluoromethoxy)benzeneHCID 59875729diisopropyl (2R,3S)-2-allyl-3-hydroxybutanedioate2×

Produkt 1

HCID 58488014diisopropyl (2S,3R)-2-hydroxy-3-{(2E)-3-[4-(trifluoromethoxy)phenyl]-2-propenyl}butanedioateAusbeute 86,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 167845palladium(II) acetateKatalysatorHCID 6342AcetonitrileLösungsmittel2×

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a solution of diisopropyl (2R,3S)-2-allyl-3-hydroxybutanedioate (Intermediate 2a, 5.0 g; 19.4 mmol; 1.0 eq.), TEA (6.23 mL; 46.5 mmol; 2.4 eq.) in CH3CN (50.0 mL) was added 1-bromo-4-(trifluoromethoxy)benzene (5.13 g; 21.3 mmol; 1.1 eq.). To this solution was added a sonicated mixture of tri-o-tolylphosphine (0.59 g; 1.94 mmol; 0.10 eq.) and palladium(II) acetate (43.46 mg; 0.19 mmol; 0.01 eq.) in CH3CN (4 mL). The reaction was stirred at 80° C. for 14 h, cooled to RT and the solvents were evaporated (rotavap). The residue was taken up in EtOAc and washed with an aqueous saturated solution of NH4Cl, an aqueous saturated solution of NaHCO3 and then with an aqueous saturated solution of NaCl and dried over MgSO4. Evaporation of the solvent gave an oil. Purification by chromatography (SiO2, gradient from 10/90 EtOAc/c-hex to 100/0 EtOAc/c-hex in 30 min.) gave a colorless oil (6.98 g, 86.2%). M+(ESI): 419.2; M−(ESI): 417.0.

Aufarbeitung

  1. additionTo this solution was added
  2. temperaturecooled to RT
  3. customthe solvents were evaporated (rotavap)
  4. washwashed with an aqueous saturated solution of NH4Cl
  5. dry with materialan aqueous saturated solution of NaHCO3 and then with an aqueous saturated solution of NaCl and dried over MgSO4
  6. customEvaporation of the solvent
  7. customgave an oil
  8. customPurification by chromatography (SiO2, gradient from 10/90 EtOAc/c-hex to 100/0 EtOAc/c-hex in 30 min.)

Quellen und Nachweise

ORD-Eintrag
ord-97e3bb616a444f8893eecbfcf1781261
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08008302B2

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