Sulfuric Acid → 3-Chloro-4-methylphenol

HRID 482962Notes

Reaction equation

HRID 482962 reaction equation
[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]

Participants

6

Procedure

283 g of 3-chloro-4-methylaniline was added to a solution of 1000 ml of water and 500 ml of concentrated sulfuric acid, causing the temperature of the mixture to rise from ambient to 95° C. The mixture was cooled and stirred at room temperature for 30 minutes, then 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. The mixture was stirred at about 5° C. for one hour, then 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. 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 3-chloro-4-methylphenol (2A).

Workup

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

Sources & evidence

ORD record
ord-18ad8c482f504d5eb4664bd00dd9789f
Source dataset
uspto-grants-1986_03
Patent number
US04577011

Reaction notes

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