Reaktion #79010

ord-a1f2bfc82ded404181b1ee54fe2ba26b

Reaktionsgleichung

CI
iodomethane
O=S(=O)([O-])[O-].[NH4+].[NH4+]
ammonium sulfate
CC1(C)OC(=O)Nc2ccc(-c3cccc(Br)c3)cc21
6-(3-bromophenyl)-4,4-dimethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one
[H-].[Na+]
sodium hydride
CN1C(=O)OC(C)(C)c2cc(-c3cccc(Br)c3)ccc21
6-(3-bromophenyl)-1,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one
Ausbeute 72.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGstirred for 1.5 hours
  2. 2
    workup.ADDITIONwas added
  3. 3
    SonstigeThe organic layer was separated
  4. 4
    Trocknendried (MgSO4)
  5. 5
    Sonstigeevaporated

Vorschrift

To a solution of 6-(3-bromophenyl)-4,4-dimethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one (1 g, 3.0 mmol) in anhydrous DMF was added, at rt under a blanket of nitrogen, sodium hydride (60% in mineral oil, 0.24 g, 6.0 mmol). After stirring for 20 minutes, the reaction solution was treated with iodomethane and stirred for 1.5 hours. The mixture was poured into a saturated aqueous ammonium sulfate solution (40 mL) and ethyl acetate (40 mL) was added. The organic layer was separated, dried (MgSO4), and evaporated to yield 6-(3-bromophenyl)-1,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one as off-white solid (0.75 g, 72%): mp 142-143° C.; 1H-NMR (DMSO-d6) δ 7.93 (s, 1H), 7.71 (m, 1H), 7.65 (s, 1H), 7.55 (d, 1H, J=8.0 Hz), 7.42 (t 1H, J=7.7 Hz), 7.18 (d, 1H, J=8.4 Hz), 3.35 (s, 3H), 1.67 (s, 6H). MS (ESI) m/z 368, 370 [M+Na]+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06713478B2uspto-grants-2004_03