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Dimethylformamide → HCID 59327230, 화합물

HRID 1880158
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HRID 1880158 반응식
[F:1][C:2]1[C:7](I)=[CH:6][CH:5]=[CH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].CN(C=O)C.[O:20]1[CH2:24][CH:23]=[CH:22][CH2:21]1>[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O>[O:20]1[CH:21]=[CH:22][CH:23]([C:7]2[C:2]([F:1])=[N:3][CH:4]=[CH:5][CH:6]=2)[CH2:24]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 155702,5-DihydrofuranHCID 70095012-Fluoro-3-iodopyridine

생성물 1

HCID 59327230HCID 59327230, 화합물

시약·촉매·용매 3

HCID 70681Tetrabutylammonium Chloride촉매
HCID 167845
palladium(II) acetate
촉매
HCID 962Water용매

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온도
25 °C

실험 절차

To a 500 mL round bottomed flask charged with 2-fluoro-3-iodopyridine (15.05 g, 67.5 mmol, Asymchem), tetrabutylammonium chloride (18.80 g, 67.6 mmol, Alfa Aesar), potassium carbonate (28.60 g, 207 mmol, Aldrich) and palladium(ii) acetate (1.48 g, 6.59 mmol, Strem) was added DMF (75 mL) followed by 2,5-dihydrofuran (50.00 mL, 678 mmol, Aldrich) and the reaction mixture was stirred vigorously at 25° C. for 2 h. The mixture was poured into 500 mL of water and the mixture was extracted with EtOAc (3×). The combined organic layers were evaporated onto silica gel and purified by flash chromatography (Isco (330 gram)) eluting with EtOAc:hexanes (0:1→1:2) to give a clear colorless oil. MS (ESI, pos. ion) m/z: 166.1 (M+1).

후처리

  1. extractionthe mixture was extracted with EtOAc (3×)
  2. customThe combined organic layers were evaporated onto silica gel
  3. custompurified by flash chromatography (Isco (330 gram))
  4. washeluting with EtOAc:hexanes (0:1→1:2)
  5. customto give a clear colorless oil

출처 및 근거

ORD 기록
ord-7577ebc502284e5d9d52617d178c2630
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318718B2

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