Acetic Acid → 6-Chloroquinazoline-2,4(1H,3H)-dione

HRID 1470138

Reaktionsgleichung

Reaktionsgleichung von HRID 1470138
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4](O)=[O:5].C(O)(=O)C.[O:16]([C:18]#[N:19])[Na].[OH-].[Na+]>O>[Cl:11][C:8]1[CH:7]=[C:3]2[C:2](=[CH:10][CH:9]=1)[NH:1][C:18](=[O:16])[NH:19][C:4]2=[O:5]

Komponenten

6

Edukt 4

HCID 176Acetic AcidHCID 124762-Amino-5-chlorobenzoic acidHCID 14798Sodium HydroxideHCID 178418852HCID 178418852, Verbindung

Produkt 1

HCID 3039986-Chloroquinazoline-2,4(1H,3H)-dione

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
30 °C

Versuchsvorschrift

Into a 500-mL 3-necked round-bottom flask, was placed a solution of 2-amino-5-chlorobenzoic acid (10 g, 58.48 mmol, 1.00 equiv) in water (100 mL), acetic acid (8 g, 133.33 mmol, 2.24 equiv). This was followed by the addition of NaOCN (8.2 g, 126.15 mmol, 2.13 equiv). The mixture was stirred for 30 mins at 30° C. To this was added sodium hydroxide (86 g, 2.15 mol, 37.00 equiv). The resulting solution was stirred overnight at 30° C. The solids were collected by filtration. The residue was dissolved in water. The pH value of the solution was adjusted to 7 with hydrogen chloride (12 mol/L). The solids were collected by filtration. This resulted in 5 g (44%) of 6-chloroquinazoline-2,4(1H,3H)-dione as a white solid.

Aufarbeitung

  1. customInto a 500-mL 3-necked round-bottom flask, was placed
  2. stirringThe resulting solution was stirred overnight at 30° C
  3. filtrationThe solids were collected by filtration
  4. dissolutionThe residue was dissolved in water
  5. filtrationThe solids were collected by filtration
  6. customThis resulted in 5 g (44%) of 6-chloroquinazoline-2,4(1H,3H)-dione as a white solid

Quellen und Nachweise

ORD-Eintrag
ord-7bc4f8ae3ee14c5c8b195591977f3ee8
Quelldatensatz
uspto-grants-2015_04
Patentnummer
US09006281B2

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