戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1753091作成日:2026年10月24日

Diisopropylethylamine → Ethyl 3-(Trifluoromethyl)pyrazole-4-carboxylate

https://huagongshe.com/ja/reaction/1753091

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Hydrazinium chlorideHCID 115031—
反応物Ethyl ethoxymethylene-3-oxo-4,4,4-trifluorobutyrateHCID 6185754—
溶媒EthanolHCID 702—
生成物Ethyl 3-(Trifluoromethyl)pyrazole-4-carboxylateHCID 596095—

反応手順

To a suspension of hydrazine hydrochloride (10 g, 147 mmol) in EtOH (500 mL), DIPEA (45.3 mL, 267 mmol) was added slowly at −20° C. and stirred for 10 minutes. Then 2-[1-ethoxy-meth-(E)-ylidene]-4,4,4-trifluoro-3-oxo-butyric acid ethyl ester (Preparation 96 Step 1, 32 g, 133.33 mmol) was added to above solution and the resulting mixture was stirred at room temperature for 16 hours. The reaction mixture was concentrated under reduced pressure and residue was partitioned between EtOAc (200 mL) and water (50 mL). The organic layer was washed with water (25 mL), dried (Na2SO4) and evaporated in vacuo. The crude material was purified by silica gel column chromatography eluting with Hexane:EtOAc 90:10 to afford the title compound as off white solid (43%, 13 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09163021B2
出典データセットuspto-grants-2015_10
ORD IDord-18b821e71bac48ef9446089e8e737330
出典メモuspto-grants-2015_10