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Triethylamine → N-(3-methoxyphenyl)pivalamide

HRID 2061449
ノート
印刷プレビュー

反応式

HRID 2061449 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([NH2:9])[CH:6]=[CH:7][CH:8]=1.C(N(CC)CC)C.[C:17](Cl)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19]>C(OCC)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([NH:9][C:17](=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19])[CH:6]=[CH:7][CH:8]=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

5

反応物 3

HCID 8471TriethylamineHCID 108243-MethoxyanilineHCID 62493Pivaloyl chloride

生成物 1

HCID 546358N-(3-methoxyphenyl)pivalamide

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
15 °C

実験手順

To an ice cooled solution of 20 g (162 mmol) 3-methoxy-phenylamine in 400 ml diethylether is added 24.9 ml (178 mmol) triethylamine and slowly within 30 minutes 23.9 ml (195 mmol) pivaloyl chloride. Due to the exothermic reaction the temperature rises despite cooling to 15° C. The temperature is left rising to room temperature, after 1 hour the reaction mixture is poured on ice and extracted with ethyl acetate, washed 2× with water and 1× with brine, dried with Na2SO4 and evaporated to give a crude product which is purified by two crystallizations from CH2Cl2/hexane to yield N-(3-methoxy-phenyl)-2,2-dimethyl-propionamide.

後処理

  1. customDue to the exothermic reaction the temperature
  2. waitThe temperature is left
  3. additionthe reaction mixture is poured on ice
  4. extractionextracted with ethyl acetate
  5. washwashed 2× with water and 1× with brine
  6. dry with materialdried with Na2SO4
  7. customevaporated
  8. customto give a crude product which
  9. customis purified by two crystallizations from CH2Cl2/hexane

出典と根拠

ORDレコード
ord-a0c48113b13e48d88f2b09e1cf8a0b0a
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08283356B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート