Reaktion #1531956

ord-d963380559a442ea9a4521d29c994e4f

Reaktionsgleichung

CCOC(C)=O
ethyl acetate
O=[N+]([O-])c1cc(CCl)cc([N+](=O)[O-])c1
3,5-Dinitrobenzyl chloride
CC1=Nc2ccc(CC(=O)O)cc2C1(C)C
2,3,3-trimethyl-3H-indol-5-yl-acetic acid
[Br-].[Na+]
sodium bromide
O=C(O)Cc1ccc2c(c1)CC=[N+]2Cc1cc([N+](=O)[O-])cc([N+](=O)[O-])c1.[Br-]
solid
Ausbeute 54.0%
O=C(O)Cc1ccc2c(c1)CC=[N+]2Cc1cc([N+](=O)[O-])cc([N+](=O)[O-])c1.[Br-]
1-(3,5-dinitrobenzyl)-5-(carboxymethyl)-3H-indolium Bromide
Ausbeute 54.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to room temperature
  2. 2
    SonstigeThe crude reaction mixture
  3. 3
    Filtrationthe dark brown solid was filtered OFF
  4. 4
    workup.DISSOLUTIONdissolved in dimethylsulfoxide before purification by reverse phase chromatography

Vorschrift

3,5-Dinitrobenzyl chloride (12.46 g, 57.5 mmol) was added to a solution of 2,3,3-trimethyl-3H-indol-5-yl-acetic acid (2.5 g, 11.5 mmol) with sodium bromide (5.92 g, 57.5 mmol) in sulfolan (10 ml). The reaction was heated at 100° C. for 20 hrs, then cooled to room temperature. The crude reaction mixture was added dropwise to an excess of ethyl acetate and the dark brown solid was filtered OFF and dissolved in dimethylsulfoxide before purification by reverse phase chromatography. The product was isolated as beige solid (54% yield). 1H NMR (d6-DMSO): δH: 8.75 (s, 1H), 8.45 (s, 2H), 7.15 (s, 1H), 6.95 (d, 1H), 6.70 (d, 2H), 5.10 (s, 2H), 3.95 (s, 2H), 3.45 (s, 3H), 1.40 (s, 6H). MALDI-TOF, m/z=398 (M+=398 for C20H20N3O6).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07662973B2uspto-grants-2010_02