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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 974028생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물FelbinacHCID 3332—
반응물Methyl iodideHCID 6328—
반응물DiisopropylamineHCID 7912—
반응물HexaneHCID 8058—
반응물Lithium diisopropylamideHCID 2724682—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물alpha-Methyl(1,1'-biphenyl)-4-acetic acidHCID 2281093%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05066666
출처 데이터셋uspto-grants-1991_11
ORD IDord-3dae1e32e66e422cb9da495ed39b06d4
출처 메모uspto-grants-1991_11