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HRID 1592872作成日:2026年10月25日

Benzene, 1-bromo-2-(trifluoromethyl)- → 1-Benzyl-4-[2-(trifluoromethyl)phenyl]piperidin-4-ol

https://huagongshe.com/reaction/1592872

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-bromo-2-(trifluoromethyl)-HCID 9806—
反応物1-Benzyl-4-piperidoneHCID 19220—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl-4-[2-(trifluoromethyl)phenyl]piperidin-4-olHCID 23294205—

反応手順

A mixture of 1.52 g of magnesium in 25 ml of THF is admixed dropwise over 20 minutes with a solution of 14.25 g of 1-bromo-2-(trifluoromethyl)benzene in 15 ml of THF and the mixture is heated at reflux for 30 minutes. After it has cooled on an ice bath, it is admixed slowly with a solution of 10 g of 1-benzyl-4-piperidinone in 30 ml of THF and left with stirring at AT for 3 hours. The reaction mixture is poured into saturated aqueous ammonium chloride solution and extracted with AcOEt, the combined organic phases are washed with water and dried over Na2SO4 and the solvents are evaporated under vacuum. The residue is chromatographed on silica gel, eluting with a DCM/AcOEt (70/30; v/v) mixture. This gives 4.5 g of the expected product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07294628B2
出典データセットuspto-grants-2007_11
ORD IDord-bb3b6b9c4c4d466d840d8feaac8154ca
出典メモuspto-grants-2007_11