Hydrochloric Acid → 2-(hydroxymethyl)-4-methoxy-6-(5-methoxy-2H-benzo[d][1,2,3]triazol-2-yl)phenol

HRID 1517765

Reaktionsgleichung

Reaktionsgleichung von HRID 1517765
[CH3:1][O:2][C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[C:5]([N+:10]([O-])=O)[CH:4]=1.Cl.[N:14]([O-])=O.[Na+].[OH-].[Na+].[OH:20][C:21]1[C:26](CO)=[CH:25][C:24]([O:29][CH3:30])=[CH:23][C:22]=1[CH2:31][OH:32].C1(O)C=CC=CC=1>O.S(=O)(=O)(O)N.C(O)C>[OH:32][CH2:31][C:22]1[CH:23]=[C:24]([O:29][CH3:30])[CH:25]=[C:26]([N:14]2[N:7]=[C:6]3[CH:8]=[CH:9][C:3]([O:2][CH3:1])=[CH:4][C:5]3=[N:10]2)[C:21]=1[OH:20]

Komponenten

10

Reaktionsbedingungen

Temperatur
-20 °C

Versuchsvorschrift

In a 500 ml round bottom flask equipped with a magnetic stirrer was added 24.8 g (148 mmol) 4-methoxy-2-nitroaniline (Aldrich), conc. HCl(aq) (J.T. Baker), 150 ml water, and 150 ml absolute ethanol. The mixture was cooled to −20° C. and a solution comprised of 10.8 (156 mmol) sodium nitrite in 40 ml water was added dropwise over 30 minutes. The reaction mixture was stirred for an additional 1 hour and then sulfamic acid (315 mg) was added to destroy excess nitrite. The undissolved solids were filtered and the filtrate containing the diazonium salt was set aside and kept cold at −10° C. NaOH (29.5 g, 739 mmol) was dissolved in 100 ml water and approximately one-fourth was added to a solution comprised of (2-hydroxy-5-methoxy-1,3-phenylene)dimethanol in 100 ml deionized water and 200 ml ethanol. The diazonium salt mixture and remaining sodium hydroxide solution were added to the reaction mixture containing the phenol derivative over a 1 hour period at 0° C. The reaction mixture was allowed to stir at 0° C. for 1 hour and ambient temperature for 3 hours. The contents were poured into 3 liters water and the pH was adjusted to 4.5 using 1N HCl. The resultant solid was filtered, washed with several liters of water, and then vacuum dried (0.1 mm Hg) at 65° C. for 20 hours using P2O5 as drying agent to afford 33.5 g (68%) of a dark solid which was used in the next step without further purification.

Aufarbeitung

  1. customIn a 500 ml round bottom flask equipped with a magnetic stirrer
  2. additionwas added dropwise over 30 minutes
  3. customto destroy excess nitrite
  4. filtrationThe undissolved solids were filtered
  5. additionthe filtrate containing the diazonium salt
  6. customkept cold at −10° C
  7. additionapproximately one-fourth was added to a solution
  8. additionwere added to the reaction mixture
  9. stirringto stir at 0° C. for 1 hour and ambient temperature for 3 hours
  10. filtrationThe resultant solid was filtered
  11. washwashed with several liters of water
  12. customvacuum dried (0.1 mm Hg) at 65° C. for 20 hours
  13. customas drying agent

Quellen und Nachweise

ORD-Eintrag
ord-6d0d0bc32567410e80bfd1de612a9386
Quelldatensatz
uspto-grants-2012_07
Patentnummer
US08232326B2

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