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HRID 1708591作成日:2026年10月26日

Dimethylformamide → Chlorfenapyr

https://huagongshe.com/reaction/1708591

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物DiethoxymethaneHCID 10024—
反応物Phosphorus oxychlorideHCID 24813—
反応物TralopyrilHCID 183559—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物ChlorfenapyrHCID 9177894.6%

反応条件

温度35 °C

反応手順

A stirred mixture of 4-bromo-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carbonitrile (17.4 g, 0.05 mole), diethoxymethane (10.4 g, 0.10 mole) and dimethylformamide (DMF) (4.6 g, 0.0625 mole) in toluene, under N2, is treated portion-wise with phosphorous oxychloride (9.6 g, 0.0625 mole) at 35°-45° C. over a 10 minute period, heated at 45°-53° C. for about 0.5 hour, cooled to 35° C. and treated dropwise with triethylamine (7.25 g, 0.0715 mole) over a 2 hour period at 35°-45° C. The reaction mixture is treated with water and the toluene is removed via azeotropic distillation. The remaining residue is treated with water, filtered and the filtercake is dried in vacuo at 60° C. to give the title product, 20.8 g, 92.7% pure, 94.6% yield, identified by HPLC analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05359090
出典データセットuspto-grants-1994_10
ORD IDord-06272aa97ad144cc9ba7983b6d33c56a
出典メモuspto-grants-1994_10