戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 612358作成日:2026年10月26日

Water → (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile

https://huagongshe.com/reaction/612358

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物(5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrileHCID 59115159—
溶媒TetrahydrofuranHCID 8028—
生成物(5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrileHCID 5444199477.2%

反応手順

5 g (22 mmol) of (5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile are dissolved in 50 ml of THF and cooled in an ice bath. After adding 4.6 ml (33 mmol) of triethylamine to the solution, 1.9 ml (24 mmol) of methanesulfonyl chloride are added dropwise, keeping the temperature below 5° C. The reaction mixture is stirred while cooling in an ice bath for 30 min. The reaction mixture is poured into 200 ml of water, and extracted with ethyl acetate. The organic phase is washed with hydrochloric acid solution and sodium chloride solution. The organic phase is dried over MgSO4, the solvent is distilled off, and the residue is purified by recrystallization from toluene. 5.2 g (77%) of (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile are obtained in the form of greenish brown crystals having a melting point of 160-162° C. (dec.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06004724
出典データセットuspto-grants-1999_12
ORD IDord-607654a676584d24bb1028defa5a2427
出典メモuspto-grants-1999_12