戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 974028作成日:2026年10月23日

Felbinac → alpha-Methyl(1,1'-biphenyl)-4-acetic acid

https://huagongshe.com/ja/reaction/974028

反応式

関与物質

役割名称HCID仕込み量
反応物FelbinacHCID 3332—
反応物Methyl iodideHCID 6328—
反応物DiisopropylamineHCID 7912—
反応物HexaneHCID 8058—
反応物Lithium diisopropylamideHCID 2724682—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物alpha-Methyl(1,1'-biphenyl)-4-acetic acidHCID 2281093%

反応手順

In usual manner, lithium diisopropylamide in tetrahydrofuran was prepared with diisopropylamine (3.2 ml, 22.6 mmol) and 1.6M n-butyllithium in hexane (14.2 ml, 22.6 mmol). ("Reagents for Organic Synthesis", 2, p. 249) To this lithium diisopropylamide in tetrahydrofuran was added dropwise 4-biphenylyl acetic acid (2.40 g, 11.3 mmol) in tetrahydrofuran at from -50° C. to -30° C. After the mixture was reacted at from -40° C. to -10° C. for 2 h, to the mixture was added dropwise methyliodide (1.77 g, 12.4 mmol) in tetrahydrofuran, then the temperature was rised at from -30° C. to room temperature in nature. After the mixture was stirred for 4 h, was added water and was adjusted at pH 2 with 3N sulfonic acid, then extracted with ether. After the ether extract was dried over, then the extract was evaporated under reduced pressure to a residue, which was chromatographed to afford 2-(4-biphenylyl)propionic acid (2.38 g, 93% yield) as white crystalline material: mp 144°-145° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05066666
出典データセットuspto-grants-1991_11
ORD IDord-3dae1e32e66e422cb9da495ed39b06d4
出典メモuspto-grants-1991_11