Ethylenediaminetetraacetic Acid → 2-Fluoro-5-(trifluoromethoxy)benzeneboronic acid

HRID 1094801노트

반응식

HRID 1094801 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]([F:12])([F:11])[F:10])=[CH:4][CH:3]=1.C(N(CC(O)=O)CC(O)=O)CN(CC(O)=O)CC(O)=O.C([Li])(CC)C.C1CCCCC1.C[O:45][B:46]([O:48]C)F>C1COCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:8][C:9]([F:10])([F:11])[F:12])=[CH:6][C:7]=1[B:46]([OH:48])[OH:45]

참가 물질

7

실험 절차

To a solution of the 4-fluoro(trifluoromethoxy)benzene (2.0 g, 11.1 mmol) in dry THF (30 ml) at −78° C., was added ethylenediaminetetraacetic acid (EDTA, 1.36 g, 11.7 mmol) followed by a 1.4 M solution of sec-butyllithium in cyclohexane (8.33 ml, 11.7 mmol) and the reaction stirred for 2 hours under nitrogen. To this reaction mixture at −78° C., was then added dropwise the preformed dimethoxyfluoroborane mixture. The reaction was stirred at −78° C. for 30 minutes, warmed to room temperature for 30 minutes, and then quenched with water (10 ml). The volume of the reaction mixture was reduced in vacuo, then the residue dissolved in diethyl ether (10 ml) and washed with an aqueous solution of 10% NaOH (50 ml). The aqueous layer was acidified and extracted with ethyl acetate (3×40 ml). The combined ethyl acetate extracts were dried over MgSO4 and concentrated in vacuo to afford the title compound as a single regioisomer (1.51 g).

후처리

  1. stirringThe reaction was stirred at −78° C. for 30 minutes
  2. customquenched with water (10 ml)
  3. dissolutionthe residue dissolved in diethyl ether (10 ml)
  4. washwashed with an aqueous solution of 10% NaOH (50 ml)
  5. extractionextracted with ethyl acetate (3×40 ml)
  6. dry with materialThe combined ethyl acetate extracts were dried over MgSO4
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-f3c42f75fae54157a96fef7ca72270f0
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08134007B2

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