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Benzene → HCID 11298596、化合物

HRID 1354202
ノート
印刷プレビュー

反応式

HRID 1354202 の反応式
[I-].C[S+](C)C.[OH-].[K+].[CH3:8][O:9][C:10]1[CH:11]=[C:12]2[C:17](=[CH:18][CH:19]=1)[N:16]=[CH:15][CH:14]=[C:13]2[CH:20]=[O:21].[CH:22]1C=CC=CC=1>C(#N)C.O>[CH3:8][O:9][C:10]1[CH:11]=[C:12]2[C:17](=[CH:18][CH:19]=1)[N:16]=[CH:15][CH:14]=[C:13]2[CH:20]1[CH2:22][O:21]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 241BenzeneHCID 14797Potassium HydroxideHCID 75127Trimethylsulfonium iodideHCID 2193126-Methoxyquinoline-4-carboxaldehyde

生成物 1

HCID 11298596HCID 11298596、化合物

試薬・触媒・溶媒 2

HCID 962Water触媒
HCID 6342
Acetonitrile
溶媒

反応条件

温度
60 °C

実験手順

Trimethylsulphonium iodide (0.954 g, 4.67 mmol) and potassium hydroxide powder (1.8 g, 32 mmol) were added to a solution of 6-methoxy-quinoline-4-carbaldehyde (0.85 g, 4.54 mmol) in acetonitrile (13.5 ml) and water (6 drops). The reaction mixture was heated at 60° C. for one hour. The mixture was then cooled to room temperature and benzene (40 ml) was added. The precipitate was filtered off and the filtrate was concentrated to dryness by rotary evaporation. The residue was diluted with water (100 ml) and ethyl acetate (100 ml), the phases were separated, and the aqueous phase was extracted twice using 50 ml of ethyl acetate each time. The combined organic phases were dried over MgSO4, filtered and concentrated to dryness by rotary evaporation. The residue was purified by column chromatography on silica gel (EtOAc).

後処理

  1. temperatureThe mixture was then cooled to room temperature
  2. filtrationThe precipitate was filtered off
  3. concentrationthe filtrate was concentrated to dryness by rotary evaporation
  4. additionThe residue was diluted with water (100 ml) and ethyl acetate (100 ml)
  5. customthe phases were separated
  6. extractionthe aqueous phase was extracted twice
  7. dry with materialThe combined organic phases were dried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated to dryness by rotary evaporation
  10. customThe residue was purified by column chromatography on silica gel (EtOAc)

出典と根拠

ORDレコード
ord-a58aa0c01b634996be0b55141b9757e8
出典データセット
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07223776B2

反応ノート

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