Veratryl alcohol → 8-Hydroxy-4-(3,4-dimethoxybenzyloxy)-2-methylquinoline

HRID 564925

反応式

HRID 564925 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH2:6][OH:7].[H-].[Na+].Cl[C:16]1[C:25]2[C:20](=[C:21]([OH:26])[CH:22]=[CH:23][CH:24]=2)[N:19]=[C:18]([CH3:27])[CH:17]=1>CN1CCN(C)C1=O>[OH:26][C:21]1[CH:22]=[CH:23][CH:24]=[C:25]2[C:20]=1[N:19]=[C:18]([CH3:27])[CH:17]=[C:16]2[O:7][CH2:6][C:5]1[CH:8]=[CH:9][C:10]([O:11][CH3:12])=[C:3]([O:2][CH3:1])[CH:4]=1

参加物

5

反応物 3

HCID 7118Veratryl alcoholHCID 24758Sodium hydrideHCID 122197224-Chloro-8-hydroxy-2-methylquinoline

生成物 1

HCID 221132868-Hydroxy-4-(3,4-dimethoxybenzyloxy)-2-methylquinoline収率 62.8%

試薬・触媒・溶媒 1

HCID 66611,3-Dimethyl-2-imidazolidinone溶媒

実験手順

To a stirred solution of 3,4-dimethoxybenzyl alcohol (1.68 g) in 1,3-dimethyl-2-imidazolidinone (10 ml) was added sodium hydride (60% in oil, 400 mg) portionwise in an ice-water bath under a nitrogen atmosphere. The mixture was stirred for 30 minutes and then 4-chloro-8-hydroxy-2-methylquinoline (770 mg) was added thereto. The reaction mixture was stirred at 150° C. for 3 hours and cooled to ambient temperature followed by partition into ethyl acetate and water. The organic layer was washed with water twice, dried over magnesium sulfate and evaporated in vacuo. The residue was washed with diethyl ether to give a pale yellow powder (812 mg) of 8-hydroxy-4-(3,4-dimethoxybenzyloxy)-2-methylquinoline.

後処理

  1. stirringThe reaction mixture was stirred at 150° C. for 3 hours
  2. customby partition into ethyl acetate and water
  3. washThe organic layer was washed with water twice
  4. dry with materialdried over magnesium sulfate
  5. customevaporated in vacuo
  6. washThe residue was washed with diethyl ether

出典と根拠

ORDレコード
ord-0b63db547e614677886d6395c8899cbc
出典データセット
uspto-grants-2001_01
特許番号
US06169095A

関連ノート

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