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

HRID 974028

반응식

HRID 974028 반응식
[CH:1]([N-]C(C)C)(C)C.[Li+].C(NC(C)C)(C)C.C([Li])CCC.CCCCCC.[C:27]1([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[CH:32]=[CH:31][C:30]([CH2:33][C:34]([OH:36])=[O:35])=[CH:29][CH:28]=1.CI>O1CCCC1.O>[C:27]1([C:37]2[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=2)[CH:28]=[CH:29][C:30]([CH:33]([CH3:1])[C:34]([OH:36])=[O:35])=[CH:31][CH:32]=1

참가 물질

9

실험 절차

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.

후처리

  1. customAfter the mixture was reacted at from -40° C. to -10° C. for 2 h, to the mixture
  2. customwas rised at from -30° C. to room temperature in nature
  3. extractionextracted with ether
  4. extractionAfter the ether extract
  5. customwas dried over, then the extract
  6. customwas evaporated under reduced pressure to a residue, which
  7. customwas chromatographed

출처 및 근거

ORD 기록
ord-3dae1e32e66e422cb9da495ed39b06d4
출처 데이터셋
uspto-grants-1991_11
특허 번호
US05066666

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