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Dimethylformamide → 2-Fluoropyridine-3-carbaldehyde

HRID 7161
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HRID 7161 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.C([N-]C(C)C)(C)C.[Li+].CN([CH:19]=[O:20])C.[NH4+].[Cl-]>C1COCC1.CCOC(C)=O>[F:1][C:2]1[C:7]([CH:19]=[O:20])=[CH:6][CH:5]=[CH:4][N:3]=1
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참가 물질

7

반응물 4

HCID 6228DimethylformamideHCID 97462-FluoropyridineHCID 25517Ammonium ChlorideHCID 2724682Lithium diisopropylamide

생성물 1

HCID 114349442-Fluoropyridine-3-carbaldehyde수율 15%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회
HCID 8857
Ethyl Acetate
용매

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온도
-78 °C

실험 절차

A solution of 2-fluoropyridine (306 mg, 3.15 mmol) in THF (1 mL) was added to a solution of lithium diisopropylamide in THF (0.20 M, 17 mL, 3.4 mmol) at −78° C. The solution was stirred at −78° C. for 4 h, then DMF (0.73 mL, 9.4 mmol) was added dropwise and stirring was continued at −78° C. for 2.5 h. Saturated NH4Cl(aq) (2 mL) was added, and the mixture was allowed to warm to room temperature. The mixture was diluted with EtOAc (20 mL), and the organic phase was washed with saturated NaHCO3(aq) (20 mL) and brine (10 mL), then dried (MgSO4) and concentrated in vacuo. Purification of the crude material by chromatography on silica gel (10% EtOAc/hexanes) gave the title compound as a yellow liquid (58 mg, 15%). 1H NMR (CDCl3) □ 7.39 (m, 1H), 8.32 (m, 1H), 8.48 (m, 1H), 10.33 (s, 1H).

후처리

  1. stirringstirring
  2. waitwas continued at −78° C. for 2.5 h
  3. temperatureto warm to room temperature
  4. washthe organic phase was washed with saturated NaHCO3(aq) (20 mL) and brine (10 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customPurification of the crude material by chromatography on silica gel (10% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-ae7961b104604450beaed78f4ad54709
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07084155B2

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