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Methyl iodide → HCID 87523600、化合物

HRID 1477196
ノート
印刷プレビュー

反応式

HRID 1477196 の反応式
[CH3:1][N:2]([CH3:18])[C:3]1([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([F:17])[CH:12]=2)[CH2:8][CH2:7][CH:6]([CH:9]=[O:10])[CH2:5][CH2:4]1.[C:19](O[K])(C)(C)C.CI>ClCCl>[CH3:1][N:2]([CH3:18])[C:3]1([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([F:17])[CH:12]=2)[CH2:8][CH2:7][C:6]([CH3:19])([CH:9]=[O:10])[CH2:5][CH2:4]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 866346814-Dimethylamino-4-(3-fluorophenyl)cyclohexanecarbaldehydeHCID 178418922HCID 178418922、化合物

生成物 1

HCID 87523600HCID 87523600、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of the title compound of step 1 (2.73 g, 10.95 mmol) in abs. dichloromethane (50 mL) was mixed with tert-BuOK (1.47 g, 13.14 mmol) and methyl iodide (747 μl, 12 mmol) at 0° C. in argon. After 30 min the batch was heated to RT and then stirred overnight (solid separated out). The reaction mixture was mixed with saturated NaCl solution (50 mL) and extracted with dichloromethane (3×30 mL). The combined organic phases were dried over Na2SO4, concentrated to low volume in a vacuum and the remaining residue was purified by flash chromatography with ethyl acetate/MeOH 20:1.

後処理

  1. custom(solid separated out)
  2. additionThe reaction mixture was mixed with saturated NaCl solution (50 mL)
  3. extractionextracted with dichloromethane (3×30 mL)
  4. dry with materialThe combined organic phases were dried over Na2SO4
  5. concentrationconcentrated to low volume in a vacuum
  6. customthe remaining residue was purified by flash chromatography with ethyl acetate/MeOH 20:1

出典と根拠

ORDレコード
ord-0da8bb2b40724bed91180d189ab66977
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09403767B2

反応ノート

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