Reaktion #2467974

ord-32927d07dc9a4b12b90a4504c6ae7db0

Reaktionsgleichung

COC(=O)c1sccc1N=NN(C)C
methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate
[Na+].[OH-]
sodium hydroxide
Cl
HCl
CN(C)N=Nc1ccsc1C(=O)O
product
Ausbeute 38.0%
CN(C)N=Nc1ccsc1C(=O)O
3-[(dimethylamino)diazenyl]thiophene-2-carboxylic acid
Ausbeute 38.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONThe mixture was diluted with ice cold water
  2. 2
    Extraktionextracted with chloroform
  3. 3
    WaschenThe combined chloroform layer was washed with water, brine
  4. 4
    Trocknendried over sodium sulfate
  5. 5
    FiltrationThe solution was filtered
  6. 6
    Sonstigeevaporated the solvent
  7. 7
    SonstigeThe residue was chromatographed over silica gel column

Vorschrift

To a solution of methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate (200 mg, 0.93 mmol) in methanol (10 mL) was added a solution of sodium hydroxide (93 mg, 2.3 mmol) in water (2 mL) and stirred at rt for 2 h. The mixture was diluted with ice cold water and acidified with dil. HCl and extracted with chloroform. The combined chloroform layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-ethyl acetate (80:20) as eluents to give the product as an off-white solid (70 mg, 38%), mp 108-110° C. IR (neat) νmax 3402, 3082, 2923, 1708, 1218, 1116, 1066, 1016, 880, 773 cm−1; 1H NMR (400 MHz, CDCl3): δ 12.21 (1H, s), 7.47 (1H, d, J=5.2 Hz), 7.30 (1H, d, J=5.2 Hz), 3.65 (3H, s), 3.28 (3H, s); LC-MS (positive ion mode): m/z 200 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08258119B2uspto-grants-2012_09