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Acetic Acid → 2-Cyano-6-methylbenzoic acid

HRID 232867
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 232867
N([O-])=O.[Na+].[NH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8](C)[C:7]=1[C:13](O)=O.S(=O)(=O)(O)O.Cl.[C:22]([OH:25])(=[O:24])[CH3:23]>O>[C:6]([C:11]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:13])[C:23]=1[C:22]([OH:25])=[O:24])#[N:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 176Acetic Acid2×HCID 313Hydrochloric AcidHCID 1118Sulfuric Acid2×HCID 1512106-Methylanthranilic acidHCID 23668193Sodium Nitrite

Produkt 1

HCID 570221172-Cyano-6-methylbenzoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel3×

Versuchsvorschrift

Under ice cooling and stirring, 1.5 g of sodium nitrite dissolved in 2 ml of water was added dropwise over 1.5 hours to 3 g of 3-amino-o-toluic acid dissolved in a mixed solution of 8 ml of acetic acid, 8.3 g of sulfuric acid and 6.5 ml of water. After 3.2 ml of acetic acid, 0.4 g of sulfuric acid and 5.6 ml of water were added to the reaction mixture, the mixture was filtered and the reaction filtrate was adjusted. On the other hand, 6.5 g of potassium cyanide dissolved in 12.7 ml of water was added dropwise to 5.9 g of copper sulfate.pentahydrate dissolved in 12.7 ml of water at room temperature under stirring and 21.5 g of sodium hydrogen carbonate and 70 ml of toluene were added to the mixture. Under ice cooling and stirring, the above reaction filtrate was added dropwise to this 10 reaction mixture over 1 hour and then the mixture was stirred at 80° C. for 30 minutes. After completion of the reaction, the reaction mixture was adjusted to about pH 3 with 1N-hydrochloric acid, crystals precipitated were extracted with ethyl acetate and the organic layer was washed with a saturated saline solution and then dried over anhydrous sodium carbonate. The solvent was removed to obtain 3.8 g of the title compound. Mass (CI); m/z=162 (M+ +1)

Aufarbeitung

  1. filtrationthe mixture was filtered
  2. dissolutionOn the other hand, 6.5 g of potassium cyanide dissolved in 12.7 ml of water
  3. additionwas added dropwise to 5.9 g of copper sulfate
  4. dissolutionpentahydrate dissolved in 12.7 ml of water at room temperature
  5. stirringunder stirring
  6. addition21.5 g of sodium hydrogen carbonate and 70 ml of toluene were added to the mixture
  7. stirringUnder ice cooling and stirring
  8. additionthe above reaction filtrate was added dropwise to this 10 reaction mixture over 1 hour
  9. stirringthe mixture was stirred at 80° C. for 30 minutes
  10. customAfter completion of the reaction
  11. customprecipitated
  12. extractionwere extracted with ethyl acetate
  13. washthe organic layer was washed with a saturated saline solution
  14. dry with materialdried over anhydrous sodium carbonate
  15. customThe solvent was removed

Quellen und Nachweise

ORD-Eintrag
ord-f2c49aa6af8e4205899da96c87f76d5c
Quelldatensatz
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05591752

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