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Dimethylformamide → tert-Butyl 6-chloropyridine-2-carboxylate

HRID 530441
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HRID 530441 반응식
[Cl:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=[O:9])[CH:5]=[CH:4][CH:3]=1.C(Cl)(=O)C(Cl)=O.CN(C=O)C.[CH3:22][C:23]([CH3:26])([O-])[CH3:24].[K+]>C(Cl)Cl>[Cl:1][C:2]1[N:7]=[C:6]([C:8]([O:10][C:23]([CH3:26])([CH3:24])[CH3:22])=[O:9])[CH:5]=[CH:4][CH:3]=1
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참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 208126-Chloropicolinic acidHCID 65578Oxalyl chlorideHCID 23665647Potassium tert-butoxide

생성물 1

HCID 53217451tert-Butyl 6-chloropyridine-2-carboxylate수율 46%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

6-Chloropyridine-2-carboxylic acid (5.00 g, 31.7 mmol) was dissolved in DCM (150 mL) and oxalyl chloride (5.45 mL, 63.5 mmol) and DMF (1 mL) were added. The reaction mixture was stirred for 3 h, concentrated in vacuo and azeotroped with DCM. The residue was dissolved in THF (150 mL) and potassium tert-butoxide (3.39 mg, 47.6 mmol) was added. The reaction mixture was stirred for 18 h, quenched with water (250 mL) and extracted with DCM (3×150 mL). The combined organic fractions were washed with sat aq NaHCO3 (150 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography to give the title compound (3.11 g, 46%) as a white solid. LCMS (ES+): 236.1 [MNa]+.

후처리

  1. concentrationconcentrated in vacuo
  2. customazeotroped with DCM
  3. dissolutionThe residue was dissolved in THF (150 mL)
  4. stirringThe reaction mixture was stirred for 18 h
  5. customquenched with water (250 mL)
  6. extractionextracted with DCM (3×150 mL)
  7. washThe combined organic fractions were washed with sat aq NaHCO3 (150 mL)
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-045fa57079654570b89dc7637da8284d
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353086B2

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