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Dimethylformamide → HCID 58668622, 화합물

HRID 2054460
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HRID 2054460 반응식
[CH3:1][C:2]([CH3:19])([CH3:18])[C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:8][N:7]=1)=[O:4].CN(C)[CH:22]=[O:23]>C1COCC1>[CH:22]([C:11]1[C:6]([NH:5][C:3](=[O:4])[C:2]([CH3:19])([CH3:18])[CH3:1])=[N:7][CH:8]=[C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:10]=1)=[O:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6228DimethylformamideHCID 47342541HCID 47342541, 화합물

생성물 1

HCID 58668622HCID 58668622, 화합물수율 67.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

2,2-dimethyl-N-(5-phenylpyridin-2-yl)propanamide (2.5 g, 9.83 mmol) was dissolved in 80 mL of dry THF and cooled to 0° C. N-Butyl lithium (2.5 M in hexanes) (9.8 mL, 24.57 mmol) was added slowly. The reaction mixture was stirred at 0° C. for 2 hours and then N,N-dimethylformamide (3.6 g, 49.15 mmol) was added. The reaction mixture was removed from the cold bath and allowed to warm to room temperature. After 30 minutes the reaction was quenched with water. The mixture was extracted with EtOAc and dried over MgSO4. The solvent was removed and the residue was chromatographed on silica gel eluting with hexanes/ethyl acetate (2:1) to afford N-(3-formyl-5-phenylpyridin-2-yl)-2,2-dimethylpropanamide (1.87 g).

후처리

  1. customThe reaction mixture was removed from the cold bath
  2. temperatureto warm to room temperature
  3. customAfter 30 minutes the reaction was quenched with water
  4. extractionThe mixture was extracted with EtOAc
  5. dry with materialdried over MgSO4
  6. customThe solvent was removed
  7. customthe residue was chromatographed on silica gel eluting with hexanes/ethyl acetate (2:1)

출처 및 근거

ORD 기록
ord-fb7edf70d5bb42998eb6cf93072fbe3d
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07329678B2

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