戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2381361作成日:2026年10月25日

[5-Chloro-6-oxo-1-(tetrahydro-pyran-2-yl)-1,6-dihydro-pyridazin-4-yl]-(2-trifluoromethyl-phenyl)-acetonitrile → 4-chloro-5-(2-trifluoromethyl-benzyl)-2H-pyridazin-3-one

https://huagongshe.com/reaction/2381361

反応式

関与物質

役割名称HCID仕込み量
反応物[5-Chloro-6-oxo-1-(tetrahydro-pyran-2-yl)-1,6-dihydro-pyridazin-4-yl]-(2-trifluoromethyl-phenyl)-acetonitrileHCID 68990773—
溶媒Acetic AcidHCID 176—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
生成物4-chloro-5-(2-trifluoromethyl-benzyl)-2H-pyridazin-3-oneHCID 6687540662%

反応条件

温度120 °C

反応手順

A mixture of [5-chloro-6-oxo-1-(tetrahydro-pyran-2-yl)-1,6-dihydro-pyridazin-4-yl]-(2-trifluoromethyl-phenyl)-acetonitrile (550 mg, 1.38 mmol) in concentrated hydrochloric acid (8.4 mL), glacial acetic acid (2.1 mL) and water (2.1 mL) (4:1:1, 0.11 M) was heated to 120° C. overnight. After this time, the reaction was cooled to 25° C. and then poured onto ice, followed by rinsing with minimal water. The resulting aqueous mixture was brought to pH=4-5 by treatment with a 4N aqueous sodium hydroxide solution. The resulting tan solids were collected by filtration. The solids were subsequently washed with water (2×10 mL) and dried in vacuo to afford 4-chloro-5-(2-trifluoromethyl-benzyl)-2H-pyridazin-3-one (0.24 g, 62%) as a tan solid; ES+-HRMS m/e calcd for C12H8N2OF3Cl [M+H+] 289.0350, found 289.0350.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08258134B2
出典データセットuspto-grants-2012_09
ORD IDord-c294e6c97af44acca8a49631cd8c51d4
出典メモuspto-grants-2012_09