戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1911316作成日:2026年10月27日

Sodium Hydroxide → 5-{4-[(Tert-butoxy)carbonyl]piperazin-1-yl}thiophene-2-carboxylic acid

https://huagongshe.com/reaction/1911316

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Tert-butyl 4-(5-formylthiophen-2-yl)piperazine-1-carboxylateHCID 28065298—
触媒Silver NitrateHCID 24470—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物5-{4-[(Tert-butoxy)carbonyl]piperazin-1-yl}thiophene-2-carboxylic acidHCID 5431345371%

反応条件

温度65 °C

反応手順

A solution of tert-butyl 4-(5-formylthien-2-yl)piperazine-1-carboxylate (2.51 g, 8.50 mmol) in ethanol (85 ml) was added in one portion to a solution of silver (I) nitrate (10.0 g, 58.8 mmol) and sodium hydroxide (4.83 g, 120.6 mmol) in water (85 ml). This mixture was stirred and heated at 65° C. for 22 h. The mixture was cooled by the addition of ice and then filtered to remove silver salts. The filtrate was carefully evaporated to remove the ethanol and the resulting aqueous solution was filtered again through a glass-fibre pad to remove tarry material. The filtrate was then diluted with water to a total volume of 400 ml and then acidified to pH 5 with acetic acid. The precipitate was filtered off, washed with water and then dried in a vacuum oven at 45° C. overnight to give 5-[4-[(2-methylpropan-2-yl)oxycarbonyl]piperazin-1-yl]thiophene-2-carboxylic acid (1.88 g, 71%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08604022B2
出典データセットuspto-grants-2013_12
ORD IDord-5d15b5d95073431c8f20077d38fdb5ca
出典メモuspto-grants-2013_12