Reacción #828716

ord-af01db63257f4f64b801d1c480a2a5e2

Ecuación de reacción

O=C1OC(=O)c2c(O)cccc21
3-Hydroxyphthalic anhydride
NN
Hydrazine
O=c1[nH][nH]c(=O)c2c(O)cccc12
5-Hydroxy-2,3-dihydrophthalazine-1,4-dione

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITAfter a few minutes
  2. 2
    Otroa white precipitate formed
  3. 3
    Filtraciónfiltered
  4. 4
    LavadoThe solids were washed with 150 mL of water
  5. 5
    Otroto dry in the air

Procedimiento

3-Hydroxyphthalic anhydride (2.0 g, 12.2 mmol, Aldrich) was stirred with 25 mL of glacial acetic acid until nearly all dissolved. Hydrazine (8.4 mL, 268 mmol) was added dropwise to the mixture. The reaction mixture fumed and became homogeneous with development of a yellow color. After a few minutes, a white precipitate formed and the yellow color faded. The mixture was stirred for three days and then filtered. The solids were washed with 150 mL of water followed by 125 mL of acetonitrile and allowed to dry in the air and then under vacuum. Yield: 2.06 g (95%). 1H NMR (DMSO-d6): δ 12.83 (s, 1H), 12.06 (s, 1H), 11.68 (s, 1H), 7.76-7.70 (t, 1H), 7.34-7.31 (d, 1H), 7.14-7.12 (d, 1H); 13C NMR (DMSO-d6): δ 163.04, 160.68, 152.74, 136.37, 126.38, 118.34, 114.50, 113.76; MS: (m/e) 178 (M+), 148, 120, 92.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05552298uspto-grants-1996_09