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

HRID 530441
ノート
印刷プレビュー

反応式

HRID 530441 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

HCID 53217451tert-Butyl 6-chloropyridine-2-carboxylate収率 46%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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]+.

後処理

  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

出典と根拠

ORDレコード
ord-045fa57079654570b89dc7637da8284d
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09353086B2

反応ノート

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