Dimethylformamide → 3-Butyl-5-fluorobenzaldehyde

HRID 20459

반응식

HRID 20459 반응식
Br[C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4](Br)[CH:3]=1.[CH2:10]([Li])[CH2:11][CH2:12][CH3:13].CN(C)[CH:17]=[O:18]>C(OCC)C>[CH2:10]([C:2]1[CH:3]=[C:4]([CH:5]=[C:6]([F:8])[CH:7]=1)[CH:17]=[O:18])[CH2:11][CH2:12][CH3:13]

참가 물질

5

실험 절차

Dissolve 1,3-Dibromo-5-fluoro-benzene (12.00 g, 0.05 mmol) in diethyl ether (470 mL) and cool to −78 C. Slowly add 1.6 M n-butyllithium in hexanes (29.5 mL, 49.6 mmol) and stir at −78 for one hour. Add dimethylformamide (3.45 g, 0.05 mmol) dropwise and warm to room temperature overnight. Quench with saturated aqueous ammonium chloride solution. Separate the layers and extract the organic layer (1×300 mL) with diethyl ether. Combine the organic layers and wash (1×150 mL) with water, (1×100 μL) with saturated aqueous sodium chloride and dry over magnesium sulfate. Purify using medium pressure chromatography (silica gel, 0-10% diethyl ether:hexanes) to give the desired product (4.15 g, 43%) as a yellow liquid.

후처리

  1. temperaturecool to −78 C
  2. customQuench with saturated aqueous ammonium chloride solution
  3. customSeparate the layers
  4. extractionextract the organic layer (1×300 mL) with diethyl ether
  5. washwash (1×150 mL) with water, (1×100 μL) with saturated aqueous sodium chloride
  6. dry with materialdry over magnesium sulfate
  7. customPurify

출처 및 근거

ORD 기록
ord-c476a40dfe7e47f582869f13e0b36cae
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07745438B2

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