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HRID 275429作成日:2026年10月27日

Pyridine → N-(4'-chloro-2'-fluoro-5'-(benzenesulphonyloxy)phenyl)-3-(trifluoromethyl)glutarimide

https://huagongshe.com/reaction/275429

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Benzenesulfonyl chlorideHCID 7369—
反応物GlutarimideHCID 70726—
反応物N-(4'-chloro-2'-fluoro-5'-hydroxyphenyl)-3-(trifluoromethyl)glutarimideHCID 15767072—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-(4'-chloro-2'-fluoro-5'-(benzenesulphonyloxy)phenyl)-3-(trifluoromethyl)glutarimideHCID 1576707182%

反応手順

To a solution of N-(4'-chloro-2'-fluoro-5'-hydroxyphenyl)-3-(trifluoromethyl)glutarimide (1.64 g, 5.05 mmol, Compound 19) in about 20 ml of methylene chloride was added via syringe nearly 2.5 eq. of pyridine (1 ml) which had been freshly distilled from CaH2. Then a solution of benzenesulfonyl chloride (0.64 ml, 5.0 mmol) in 4.5 ml of methylene chloride was slowly added dropwise to the reaction mixture with ice bath cooling. The reaction mixture was allowed to warm to room temperature and stirred for 12 hours. Then there was added 0.17 g of additional glutarimide and the reaction mixture was stirred at room temperature for an additional 12 hours. The reaction mixture was poured into 50 ml of water and the layers were separated. The organic layer was evaporated in vacuo and the residue was dried in the vacuum oven (20-50 Torr, 50° C.). The resulting brown solid was rinsed with approximately 5 ml of methylene chloride and suction filtered to yield 1.9 g (82% yield) of the desired product as an off-white powder (m.p. 214°-215° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05393735
出典データセットuspto-grants-1995_02
ORD IDord-7c28fb228d664c3b89d96d1292f1ea9d
出典メモuspto-grants-1995_02