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Dimethylformamide → Methyl 2-chloro-6-methylpyridine-3-carboxylate

HRID 347628
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HRID 347628 반응식
[Cl:1][C:2]1[N:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12]N(C=O)C.C(Cl)(=O)C(Cl)=O>ClCCl>[Cl:1][C:2]1[N:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:12])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 1217242-Chloro-6-methylnicotinic acid

생성물 1

HCID 13055804Methyl 2-chloro-6-methylpyridine-3-carboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a suspension of 2-chloro-6-methylnicotinic acid (5.3 g, 30.8 mmol) in dichloromethane (100 ml) at 0° C. were added DMF (1 ml) and oxalyl chloride (3.2 ml, 36.9 mmol). The mixture was allowed to warmn to room temperature and stirred for 5 h. The solvents were removed in vacuo and the residue was dissolved in dichloromethane (50 ml) and methanol (50 ml). The mixture was stirred at room temperature for 18 h and then concentrated in vacuo. The residue was dissolved in chloroform, washed with saturated sodium bicarbonate solution and brine, dried over MgSO4, and concentrated in vacuo to give a brown oil; yield 5.70 g (100%).

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후처리

  1. customto warmn to room temperature
  2. customThe solvents were removed in vacuo
  3. dissolutionthe residue was dissolved in dichloromethane (50 ml)
  4. stirringThe mixture was stirred at room temperature for 18 h
  5. concentrationconcentrated in vacuo
  6. dissolutionThe residue was dissolved in chloroform
  7. washwashed with saturated sodium bicarbonate solution and brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated in vacuo
  10. customto give a brown oil

출처 및 근거

ORD 기록
ord-e8a38c9878e446839eb2daf1c59b6e4a
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07176195B2

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