Reaktion #1561466

ord-cf5d182b7a704745bea2c068a7c9aec3

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas microwaved 10 min at 100° C
  2. 2
    SonstigeThe reaction was quenched with water
  3. 3
    Extraktionextracted with EtOAc
  4. 4
    WaschenThe organic layer was washed with brine
  5. 5
    Sonstigedried
  6. 6
    Einengenconcentrated
  7. 7
    SonstigeThe residue was purified with prep-HPLC

Vorschrift

A mixture of (5-bromo-3,4-dihydro-1H-isochromen-1-yl)methanol (390 mg, 1.6 mmol), Zn(CN)2 (113 mg, 0.960 mmol), TMEDA (0.37 mg), xantphose (4.6 mg) and Pd(dba)3 (2.6 mg) in anhydrous DMF was microwaved 10 min at 100° C. The reaction was quenched with water and extracted with EtOAc. The organic layer was washed with brine, dried and concentrated. The residue was purified with prep-HPLC to give 1-(hydroxymethyl)-3,4-dihydro-1H-isochromene-5-carbonitrile. 1H-NMR (400 MHz, CDCl3) δ: 7.49˜7.50 (m, 1H), 7.24˜7.48 (m, 2 H), 4.76˜4.78 (m, 1H), 4.17˜4.22 (m, 1H), 3.76˜3.95 (m, 3H), 3.01˜3.09 (m, 1H), 2.89˜2.95 (m, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09018211B2uspto-grants-2015_04