Ethyl bromoacetate → (2-chloro-5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluorophenoxy)acetic acid, ethyl ester

HRID 1198418Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1198418
[Cl:1][C:2]1[C:3]([C:12]2[CH:17]=[C:16]([OH:18])[C:15]([Cl:19])=[CH:14][C:13]=2[F:20])=[N:4][N:5]([CH3:11])[C:6]=1[C:7]([F:10])([F:9])[F:8].C([O-])([O-])=O.[K+].[K+].Br[CH2:28][C:29]([O:31][CH2:32][CH3:33])=[O:30]>CC(C)=O>[Cl:19][C:15]1[CH:14]=[C:13]([F:20])[C:12]([C:3]2[C:2]([Cl:1])=[C:6]([C:7]([F:8])([F:10])[F:9])[N:5]([CH3:11])[N:4]=2)=[CH:17][C:16]=1[O:18][CH2:28][C:29]([O:31][CH2:32][CH3:33])=[O:30]

Komponenten

5

Edukt 3

HCID 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 111210244-Chloro-3-(4-chloro-2-fluoro-5-hydroxyphenyl)-1-methyl-5-trifluoromethyl-1H-pyrazole

Produkt 1

HCID 86747522(2-chloro-5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluorophenoxy)acetic acid, ethyl esterAusbeute 100 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

At 25° C., 13.16 g (0.04 mole) 4-chloro-3-(4-chloro-2-fluoro-5-hydroxyphenyl)-1-methyl-5-(trifluoromethyl)-1H-pyrazole, 6.1 g (0.044 mole) K2CO3, and 4.8 mL (0.044 mole) ethyl bromoacetate were slurried in 25 mL acetone. The reaction mixture was stirred at 25° C. for 16 hours. The reaction solution was poured into 150 mL ice water, filtered, washed with water and air dried. The residue was recrystallized from hexane to give 16.6 g (100%) of (2-chloro-5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluorophenoxy)acetic acid, ethyl ester as a white solid, mp 130°-131° C.

Aufarbeitung

  1. customAt 25° C.
  2. filtrationfiltered
  3. washwashed with water and air
  4. customdried
  5. customThe residue was recrystallized from hexane

Quellen und Nachweise

ORD-Eintrag
ord-95486a63f9524460b152930535daed88
Quelldatensatz
uspto-grants-1994_01
Patentnummer
US05281571

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