Reaktion #350989

ord-d9bfded6615342a1bfb8213e25ec4660

Reaktionsgleichung

OCCC(c1ccccc1)(c1ccccc1)c1ccccc1
triphenylpropanol
O=C(O)Cc1ccc(O)cc1
4-hydroxyphenylacetic acid
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCOC(=O)/N=N/C(=O)OCC
DEAD
O=C(Cc1ccc(O)cc1)OCCC(c1ccccc1)(c1ccccc1)c1ccccc1
3,3,3-Triphenylpropyl 2-(4-hydroxyphenyl)acetate
Ausbeute 34.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe THF was evaporated
  2. 2
    SonstigeThe residue was chromatographed on silica gel using 15-30% EtOAc/hexanes

Vorschrift

To triphenylpropanol (3.98 mmol), 4-hydroxyphenylacetic acid (3.98 mmol), and triphenylphosphine (4.39 mmol) in dry THF (20 mL) at 0° C. under a nitrogen atmosphere, was added DEAD (4.39 mmol) in dry THF (20 mL) over 15 minutes. The reaction was stirred at room temperature for 16 h and then the THF was evaporated. The residue was chromatographed on silica gel using 15-30% EtOAc/hexanes. White solid, mp=136°-138° C. (ether), 34% yield. 1H NMR δ 7.15-7.27 (m, 15H), 7.10 (d, J=8.5 Hz, 2H), 6.77 (d, J=8.5 Hz, 2H), 4.90 (s, 1H), 3.90 (t, J=7.9 Hz, 2H), 3.47 (s, 2H), 2.93 (t, J=7.9 Hz, 2H). Anal. calcd. for C29H26O3 : C, 82.44; H, 6.20. Found: C, 82.29; H, 6.24.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05643950uspto-grants-1997_07