Dimethyl Sulfate → Methyl 2-chloro-6-fluorobenzthioimidate

HRID 2269660Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2269660
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([F:11])[C:3]=1[C:4](=[S:6])[NH2:5].[CH3:12]OS(OC)(=O)=O>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([F:11])[C:3]=1[C:4]([S:6][CH3:12])=[NH:5]

Komponenten

4

Versuchsvorschrift

Into a 25-mL three-necked round bottom flask equipped with a magnetic stirrer was added 2-chloro-6-fluorobenzthioamide (1.89 g, 10.0 mmol) and toluene (10 mL). Dimethylsulfate was added dropwise and the mixture was allowed to stir at reflux using a Dean Stark trap. The solids were removed via filtration and washed with small portions of toluene to give methyl 2-chloro-6-fluorobenzthioimidate as a light yellow solid: 2.7 g (87% yield): 1H NMR (DMSO-d6) δ7.7 (m, 1H), 7.5 (m, 2H), 3.3 (s, 3H), 2.7 (s, 3H); 98% pure by HPLC analysis.

Aufarbeitung

  1. customInto a 25-mL three-necked round bottom flask equipped with a magnetic stirrer
  2. temperatureat reflux
  3. customThe solids were removed via filtration
  4. washwashed with small portions of toluene

Quellen und Nachweise

ORD-Eintrag
ord-55fb770f5e5144e88630ef3b1e3b4cc6
Quelldatensatz
uspto-grants-2001_12
Patentnummer
US06329528B1

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