戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 238659作成日:2026年10月27日

Triethylamine → HCID 68745534、化合物

https://huagongshe.com/reaction/238659

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-ChlorostyreneHCID 14906—
反応物Sodium HypochloriteHCID 23665760—
反応物4-[4-[(hydroxyimino)methyl]-2-thiazolyl]-1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]piperidineHCID 86631243—
溶媒DichloromethaneHCID 6344—
生成物HCID 68745534HCID 68745534—

反応手順

To a solution of 1-chloro-2-ethenylbenzene (0.035 g, 0.25 mmol), triethylamine (2.5 mg, 0.025 mmol) and Clorox® aqueous sodium hypochlorite solution (1 mL, 16.1 mmol) in dichloromethane (5 mL) was added 4-[4-[(hydroxyimino)methyl]-2-thiazolyl]-1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]piperidine (i.e. the product of Example 2, Step C) (0.10 g, 0.25 mmol) in dichloromethane (5 mL) dropwise over 1 h at 0° C. The reaction mixture was allowed to stir for 1 h, then filtered through Celite® diatomaceous filter aid, and concentrated under reduced pressure to give an oil, which was purified by column chromatography on silica gel using 50% ethyl acetate in hexane as eluant to give 73 mg of the title compound as a white foam, melting at 115-122° C. (crystallized from methyl acetate/petroleum ether).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642634B2
出典データセットuspto-grants-2014_02
ORD IDord-aaf7e68db93d44ffb6098f5868039269
出典メモuspto-grants-2014_02