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HRID 1720461作成日:2026年10月26日

1,1-Dichloro-1-fluoromethanesulfenyl chloride → 1-(2,6-Dichloro-4-trifluoromethylphenyl)-2,5-dimethyl-3-(dichlorofluoromethylthio)pyrrole

https://huagongshe.com/reaction/1720461

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-Dichloro-1-fluoromethanesulfenyl chlorideHCID 75926—
反応物1-(2,6-Dichloro-4-trifluoromethylphenyl)-2,5-dimethylpyrroleHCID 22418322—
溶媒DichloromethaneHCID 6344—
生成物1-(2,6-Dichloro-4-trifluoromethylphenyl)-2,5-dimethyl-3-(dichlorofluoromethylthio)pyrroleHCID 2241832890%

反応条件

温度0 °C

反応手順

To a cooled (0° C.) solution of 3.00 g (9.74 mmoles) of the 1-(2,6-dichloro-4-trifluoromethylphenyl)-2,5-dimethylpyrrole prepared above in 60 mL of dichloromethane was added dropwise 1.03 mL (1.67 g, 9.86 mmoles) of dichlorofluoromethanesulfenyl chloride in 5 mL of dichloromethane solution. The mixture was maintained at 0° C. for 3 hours and then washed with a saturated aqueous solution of NaHCO3. Removal of solvent under reduced pressure afforded a black off which was chromatographed on silica gel with a 1% EtOAc in hexane eluent to give 3.85 g (90%) of 1-(2,6-dichloro-4-trifluoromethylphenyl)-2,5-dimethyl-3-(dichlorofluoromethylthio)pyrrole as a yellow off: 1H NMR (CDCl3): δ2.00 (s, 3H), 2.10 (s, 3H), 6.27 (s, 1H), 7.80 (s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05506260
出典データセットuspto-grants-1996_04
ORD IDord-4823b68e3cc74b5e8fba5df2573b3a18
出典メモuspto-grants-1996_04