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Potassium Iodide → Quinoline-6-carboxylic acid oxiranylmethyl ester

HRID 720882
ノート
印刷プレビュー

反応式

HRID 720882 の反応式
[N:1]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([OH:13])=[O:12])=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH2:14]([CH:16]1[O:18][CH2:17]1)Cl.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CN(C=O)C>[O:18]1[CH2:17][CH:16]1[CH2:14][O:12][C:11]([C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[N:1]=[CH:2][CH:3]=[CH:4]2)=[O:13]
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 4875Potassium IodideHCID 7835EpichlorohydrinHCID 11430Potassium CarbonateHCID 825716-Quinolinecarboxylic acid

生成物 1

HCID 12020264Quinoline-6-carboxylic acid oxiranylmethyl ester収率 21.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

Quinoline-6-carboxylic acid (1 g; 5.78 mmol) is dissolved in DMF (10 mL) at ambient temperature. Epichlorohydrin (0.4517 mL; 5.59 mmol) is added followed by mortar ground potassium carbonate (0.80 g; 5.79 mmol). The mixture is stirred at ambient temperature for 48 hours. Potassium iodide (96 mg; 0.58 mmol) is added and stirring is continued at ambient temperature for 24 hours. The mixture is heated to 60° C. and maintained for 72 hours. After cooling, the mixture is poured onto water (700 mL) and extracted with ethyl acetate (3×100 mL). The combined organic extracts are washed successively with water (100 mL), and brine (50 mL), then dried over MgSO4, filtered, and concentrated in vacuo at 30 C. The residue is purified via silica gel chromatography with gradient elution (20%→67% ethyl acetate in hexanes) affording the desired product (270 mg) as a white solid. ESMS:MH+ 230.0 (base).

後処理

  1. stirringstirring
  2. waitis continued at ambient temperature for 24 hours
  3. temperatureThe mixture is heated to 60° C.
  4. temperaturemaintained for 72 hours
  5. temperatureAfter cooling
  6. additionthe mixture is poured onto water (700 mL)
  7. extractionextracted with ethyl acetate (3×100 mL)
  8. washThe combined organic extracts are washed successively with water (100 mL), and brine (50 mL)
  9. dry with materialdried over MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo at 30 C
  12. customThe residue is purified via silica gel chromatography with gradient elution (20%→67% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-c597ed8ffc5440bfb0bf63008421358f
出典データセット
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07135483B2

反応ノート

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