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Potassium Carbonate → 8-Chloro-7-(2-methoxyethoxy)-2-methylquinoline

HRID 339000
ノート
印刷プレビュー

反応式

HRID 339000 の反応式
[Cl:1][C:2]1[C:3]([OH:13])=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([CH3:12])[CH:8]=[CH:7]2.C(=O)([O-])[O-].[K+].[K+].Br[CH2:21][CH2:22][O:23][CH3:24]>CC(C)=O>[Cl:1][C:2]1[C:3]([O:13][CH2:21][CH2:22][O:23][CH3:24])=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([CH3:12])[CH:8]=[CH:7]2
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 11430Potassium CarbonateHCID 809722-Bromoethyl methyl etherHCID 1358589748-Chloro-2-methylquinolin-7-ol

生成物 1

HCID 709830998-Chloro-7-(2-methoxyethoxy)-2-methylquinoline

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

8-chloro-2-methylquinolin-7-ol (80 mg, 0.41 mmol), potassium carbonate (171 mg, 1.2 mmol) and 1-bromo-2-methoxyethane (115 mg, 0.83 mmol) in acetone (10 mL) were stirred at 70° C. in a sealed tube for 20 hours. After dilution with water (50 mL) the reaction was extracted with DCM. The DCM phases were concentrated under reduced pressure and the residue purified by reverse phase chromatography (SP4, 25M, eluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes) to yield 8-chloro-7-(2-methoxyethoxy)-2-methylquinoline as a solid.

後処理

  1. extractionAfter dilution with water (50 mL) the reaction was extracted with DCM
  2. concentrationThe DCM phases were concentrated under reduced pressure
  3. customthe residue purified by reverse phase chromatography (SP4, 25M
  4. washeluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes)

出典と根拠

ORDレコード
ord-cb6694d9264d478d9c5d886681ebee4d
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889704B2

反応ノート

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