戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 637251作成日:2026年10月27日

5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chloride → N-[5-(o-chloro-p-trifluoromethyl-phenoxy)-2-nitrobenzoyl]-S,S-dimethyl-sulphoximine

https://huagongshe.com/reaction/637251

反応式

関与物質

役割名称HCID仕込み量
反応物5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chlorideHCID 3017765—
反応物Dimethyl sulphoximine potassium saltHCID 86740516—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物N-[5-(o-chloro-p-trifluoromethyl-phenoxy)-2-nitrobenzoyl]-S,S-dimethyl-sulphoximineHCID 20256523—

反応手順

A solution of 38.01 g of 5-(o-chloro-p-trifluoromethyl-phenoxy)-2-nitrobenzoyl chloride in 125 ml of absolute 1,2-dimethoxyethane is added dropwise at 10°-15° C. while stirring during 30 minutes to a suspension of the dimethyl sulphoximine potassium salt in 250 ml of absolute 1,2-dimethoxyethane. The mixture is stirred at room temperature for 24 hours and subsequently evaporated to dryness under reduced pressure. The resinous residue is dissolved in 1.25 l of diethyl ether, the solution is filtered through Celite and the filtrate is evaporated to dryness. The residue is subsequently purified by chromatography on silica gel with methylene chloride. There is obtained N-[5-(o-chloro-p-trifluoromethyl-phenoxy)-2-nitrobenzoyl]-S,S-dimethyl-sulphoximine as colourless crystals, m.p. 126°-127° C.; 1H-NMR (CDCl3): 7.99 (d,1H), 7.80 (d,1H), 7.60 (q,1H), 7.23 (d,1H) 7.14 (d,1H), 7.02 (q,1H) and 3.40 (s,6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04556413
出典データセットuspto-grants-1985_12
ORD IDord-53afbfdcc1b94f9780874c728e0acec5
出典メモuspto-grants-1985_12