Reaktion #7811

ord-1bb2abbd51504100ae8fddcf2916a41c

Reaktionsgleichung

COCOc1cc(-c2nc3ccccc3o2)ccc1CBr
2-[4-(Bromomethyl)-3-(methoxymethoxy)phenyl]-1,3-benzoxazole
[C-]#N.[Na+]
sodium cyanide
CCOC(C)=O
EtOAc
COCOc1cc(-c2nc3ccccc3o2)ccc1CC#N
[4-(1,3-benzoxazol-2-yl)-2-(methoxymethoxy)phenyl]acetonitrile

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenThe EtOAc solution was washed with H2O (2×20 mL), brine (2×20 mL)
  2. 2
    Trocknendried (MgSO4)
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated in vacuo
  5. 5
    WaschenThe residue was eluted with flash column (silica gel, hexanes:EtOAc 4:1)

Vorschrift

2-[4-(Bromomethyl)-3-(methoxymethoxy)phenyl]-1,3-benzoxazole (250 mg, 0.72 mmol) was treated with sodium cyanide (150 mg, 2.2 mmol) in DMF/H2O (15 mL/1.5 mL) at 90° C. for 3 h and EtOAc (150 mL) was added. The EtOAc solution was washed with H2O (2×20 mL), brine (2×20 mL), dried (MgSO4), filtered, and concentrated in vacuo. The residue was eluted with flash column (silica gel, hexanes:EtOAc 4:1) to afford the desired [4-(1,3-benzoxazol-2-yl)-2-(methoxymethoxy)phenyl]acetonitrile as a yellow solid. 1H NMR (CD3OD, 300 MHz), δ 8.02 (d, 2H), 7.95 (m, 1H), 7.80 (m, 1H), 7.63 (m, 1H), 7.57 (d, 2H), 7.40 (m, 2H). MS (ESI) 295 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087601B2uspto-grants-2006_08