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HRID 1886309作成日:2026年10月27日

Triethylamine → alpha-Pivaloyl-alpha-[4-(3-hydroxypropyl)pyrazolyl]-2-chloroacetanilide

https://huagongshe.com/reaction/1886309

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-(1H-pyrazol-4-yl)propan-1-olHCID 3578384—
反応物alpha-Bromo-2-pivaloyl-2-chloroacetanilideHCID 19875675—
溶媒ChloroformHCID 6212—
生成物alpha-Pivaloyl-alpha-[4-(3-hydroxypropyl)pyrazolyl]-2-chloroacetanilideHCID 17844708787.4%

反応手順

56.7 g of 4-(3-hydroxypropyl)pyrazole and 45.5 g of triethylamine were dissolved in 500 ml of chloroform and, under cooling with ice, a solution of 88.8 g of α-bromo-2-pivaloyl-2-chloroacetanilide in 300 ml of chloroform was dropwise added thereto in about 1 hour. After completion of the dropwise addition, the solution was stirred for 2 hours, and the reaction solution was washed twice with 300 ml of dilute hydrochloric acid, then twice with 500 ml of water. The reaction solution was dried with anhydrous sodium sulfate, concentrated, and purified by silica gel chromatography to obtain 88.2 g of oily α-pivaloyl-α-[4-(3-hydroxypropyl)pyrazolyl]-2-chloroacetanilide. (Yield: 78%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05151356
出典データセットuspto-grants-1992_09
ORD IDord-610ee9c4254941dbac0af0a4b1cf4cb2
出典メモuspto-grants-1992_09