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HRID 13764作成日:2026年10月24日

Ammonium Chloride → 4-(1-Methylpiperidin-4-yloxy)-3-trifluoromethylbenzonitrile

https://huagongshe.com/ja/reaction/13764

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物4-Piperidinol, 1-methyl-HCID 66048—
反応物4-Fluoro-3-(trifluoromethyl)benzonitrileHCID 144255—
反応物Potassium tert-butoxideHCID 23665647—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-(1-Methylpiperidin-4-yloxy)-3-trifluoromethylbenzonitrileHCID 2314594064.8%

反応手順

6.68 g of potassium t-butoxide was suspended in 40 ml of anhydrous tetrahydrofuran and a solution of 6.85 g of 1-methyl-4-hydroxypiperidine in 20 ml of anhydrous tetrahydrofuran was added dropwise over 35 minutes while stirring under ice-water cooling and further the mixture was stirred for 30 minutes. On the other hand, 7.50 g of 4-fluoro-3-trifluoromethylbenzonitrile was dissolved in 40 ml of anhydrous tetrahydrofuran, the mixture was stirred under cooling in a dry ice/acetone bath, and the solution prepared earlier was added dropwise at the internal temperature of −70° C. After adding dropwise, the reaction solution was stirred overnight while naturally heating up to room temperature. The reaction solution was ice-cooled, an aqueous saturated ammonium chloride solution and water were added thereto, and then the solvent was distilled off under reduced pressure. The residue was subjected to extraction with ethyl acetate twice. The extracts were washed in turn with water and saturated saline and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 7.31 g of the objective compound as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728131B2
出典データセットuspto-grants-2010_06
ORD IDord-ac5ac920425a4ccd89ccd021d933c772
出典メモuspto-grants-2010_06