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HRID 2290697作成日:2026年10月26日

Toluene → Diflufenican

https://huagongshe.com/reaction/2290697

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2,4-DifluoroanilineHCID 9709—
反応物Thionyl ChlorideHCID 24386—
反応物2-(3-(Trifluoromethyl)phenoxy)-3-pyridinecarboxylic acidHCID 215891—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物DiflufenicanHCID 91735—

反応手順

A mixture of thionyl chloride (465 ml) and 2-(3-trifluoromethylphenoxy)nicotinic acid [930 L g; described by F. J. Villani et al, J. Med. Chem. 18, 1 (1975)] was allowed to stand at ambient temperature for 18 hours and was then heated at reflux for 1 hour. Toluene (1 liter) was then added and the solution was evaporated under reduced pressure. The residue thus obtained was dissolved in methylene chloride (3 liters) and treated, with stirring, with triethylamine (453 ml) at ambient temperature. 2,4-Difluoroaniline (422 g) was then added over 1 hour while maintaining the temperature at 10° to 15° C. and the mixture was then heated at reflux for 2 hours. The methylene chloride was removed by distillation and the residue was treated with water (4 liters). A solid of spongy texture was obtained which was filtered off, dried at 50° C. and recrystallised from a mixture of toluene and hexane (2:3; 15 liters), to give N-(2,4-difluorophenyl)-2-(3-trifluoromethylphenoxy)nicotinamide (720 g), m.p. 160°-161° C. as a colourless crystalline solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04618366
出典データセットuspto-grants-1986_10
ORD IDord-49dfd793623541d7ac8cb8e2b91c85ec
出典メモuspto-grants-1986_10