Toluene → (4-chloro-2-Methylphenoxy)acetic acid

HRID 431807

Reaktionsgleichung

Reaktionsgleichung von HRID 431807
[C:1](=[O:4])(O)[O-:2].[Na+].[CH3:6][O:7][C:8]1[CH:13]=[CH:12]C(N)=CC=1.Cl[CH2:16][CH2:17][C:18]([Cl:20])=O.[C:21]1(C)C=CC=CC=1>>[CH3:21][C:13]1[CH:12]=[C:18]([Cl:20])[CH:17]=[CH:16][C:8]=1[O:7][CH2:6][C:1]([OH:2])=[O:4]

Komponenten

5

Versuchsvorschrift

In the most preferred of these processes, p-anisidine is dissolved in a sufficient amount of toluene to produce an approximately 3 to 5 M solution, more preferably about 4 M solution. Between 1 and 2 equivalents, more preferably about 1.5 equivalents, of sodium bicarbonate (“NaHCO3”) are suspended in the p-anisidine solution and the resulting suspension is stirred while an approximately equivalent amount 3-chloropropionyl chloride (i.e. 1-1.2 eq.) is added dropwise to the stirred suspension. The addition may be conducted at reduced or ambient temperature and the temperature may be allowed to rise, but should not be allowed to exceed 70° C. After completing the addition, the temperature of the reaction is maintained at between room temperature and the reflux temperature of toluene (111° C.), most preferrably about 60° C., for a time sufficient for the reaction to be complete. Progress of the reaction may be monitored by TLC using the method described in Example 2a. After the reaction is complete, the reaction mixture is quenched with water or aqueous mineral acid and MCPA is isolated from the resulting suspension by filtration, decantation and the like, preferably filtration. The MCPA is then washed with water, toluene, or other nonviscous liquid in which the MCPA is not substantially soluble. The washed solid is then dried.

Aufarbeitung

  1. additionis added dropwise to the stirred suspension
  2. additionThe addition
  3. customambient temperature
  4. customto exceed 70° C
  5. additionthe addition
  6. customProgress of the reaction
  7. customthe reaction mixture is quenched with water or aqueous mineral acid

Quellen und Nachweise

ORD-Eintrag
ord-80d3a4aa02ca4801bbcfc5b3d7201cd6
Quelldatensatz
uspto-grants-2003_12
Patentnummer
US06660773B2

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