Sulfuric Acid → 3-Chloro-4-methylphenol

HRID 279894

Reaktionsgleichung

Reaktionsgleichung von HRID 279894
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[CH3:9])N.S(=O)(=O)(O)[OH:11].N([O-])=O.[Na+].CCCCCC>O>[Cl:1][C:2]1[CH:3]=[C:4]([OH:11])[CH:6]=[CH:7][C:8]=1[CH3:9]

Komponenten

6

Versuchsvorschrift

283.0 g of 3-chloro-4-methylaniline, 1000 ml of water and 500 ml of concentrated sulfuric acid were mixed, initially at room temperature. The temperature of the mixture rose to 95° C. The mixture was stirred at room temperature for 30 minutes, cooled to 5° C. and a solution of 145 g of sodium nitrite in 500 ml of water was slowly added (1.5 hours) to the stirred mixture at 5°-10° C., then the mixture was stirred at about 5° C. for one hour. The resulting solution was added over two hours to a stirred solution of 1.2 liters of concentrated sulfuric acid in 2 liters of water, at 105°-110° C., and the resulting mixture was stirred at 110° C. for one hour, then held at room temperature for 18 hours. Then 3.5 liters of hexane was added, the mixture was stirred for 30 minutes, allowed to stand, and the two liquid phases were separated. The hexane phase was filtered, washed with water, dried (MgSO4) and concentrated to dryness to give crude (91%) 3-chloro-4-methylphenol (3A).

Aufarbeitung

  1. customrose to 95° C
  2. temperaturecooled to 5° C.
  3. stirringthe mixture was stirred at about 5° C. for one hour
  4. stirringthe resulting mixture was stirred at 110° C. for one hour
  5. waitheld at room temperature for 18 hours
  6. stirringthe mixture was stirred for 30 minutes
  7. customthe two liquid phases were separated
  8. filtrationThe hexane phase was filtered
  9. washwashed with water
  10. dry with materialdried (MgSO4)
  11. concentrationconcentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-478c206ea42a483fa46925d58f2b01fd
Quelldatensatz
uspto-grants-1986_05
Patentnummer
US04587259

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