Ethanol → N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide

HRID 1644056

反応式

HRID 1644056 の反応式
[OH-].[K+].[OH:3][C:4]1[CH:19]=[CH:18][C:7]([C:8]([NH:10][CH:11]([CH2:15][CH2:16][CH3:17])[CH2:12][CH2:13][CH3:14])=[O:9])=[CH:6][C:5]=1[CH3:20].Cl[CH:22]([OH:24])[CH3:23].[CH2:25](O)C>>[CH3:17][CH2:16][CH2:15][CH:11]([NH:10][C:8](=[O:9])[C:7]1[CH:18]=[CH:19][C:4]([O:3][CH2:23][CH2:22][O:24][CH3:25])=[C:5]([CH3:20])[CH:6]=1)[CH2:12][CH2:13][CH3:14]

参加物

5

反応物 4

HCID 702EthanolHCID 14797Potassium HydroxideHCID 126390351-Chloroethan-1-olHCID 575277684-hydroxy-3-methyl-N-(1-propyl-butyl)-benzamide

生成物 1

HCID 57527906N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide収率 39%

反応条件

温度
80 °C

実験手順

Potassium hydroxide (4 mmol) was dissolved in ethanol (5 mL) and heated at 80° C. 4-hydroxy-3-methyl-N-(1-propyl-butyl)-benzamide (example 58) (1 mmol) was added into the solution followed by chloroethanol (3 mmol). The reaction was stirred overnight at 80° C. The reaction mixture was concentrated down and dissolved in 5% citric acid. the mixture was stirred for 1 hour. The aqueous mixture was extracted three times with ethyl acetate. The combined ethyl acetate was washed with water and dried down over sodium sulfate. The organic layer was concentrated down and purified by HPLC to yield 39% of N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide. MS (M+H, 308.25).

後処理

  1. concentrationThe reaction mixture was concentrated down
  2. dissolutiondissolved in 5% citric acid
  3. stirringthe mixture was stirred for 1 hour
  4. extractionThe aqueous mixture was extracted three times with ethyl acetate
  5. washThe combined ethyl acetate was washed with water
  6. dry with materialdried down over sodium sulfate
  7. concentrationThe organic layer was concentrated down
  8. custompurified by HPLC

出典と根拠

ORDレコード
ord-a99ddfc8bf2a4c96918318e8b2828930
出典データセット
uspto-grants-2012_02
特許番号
US08124121B2

関連ノート

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