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6-Aminohexanoic Acid → 6-Maleimidohexanoic acid

HRID 1017121
ノート
印刷プレビュー

反応式

HRID 1017121 の反応式
[C:1]1(=O)[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[CH2:8]([CH2:14][CH2:15][NH2:16])[CH2:9][CH2:10][C:11]([OH:13])=[O:12]>C(O)(=O)C>[C:1]1(=[O:6])[N:16]([CH2:15][CH2:14][CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])[C:4](=[O:5])[CH:3]=[CH:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 5646-Aminohexanoic AcidHCID 7923Maleic Anhydride

生成物 1

HCID 5736836-Maleimidohexanoic acid収率 75.8%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒3 回

実験手順

A solution of maleic anhydride (0.05 mole) in acetic acid (20 mL) was mixed with a solution of ε-Amino-n-caproic acid (0.05 mole) in acetic acid (50 mL) and stirred at room temperature for 2 hours. An additional amount of acetic acid (150 mL) was added and the reaction mixture refluxed for 16 hours. The reaction mixture was evaporated under vacuo to an oil and chloroform was then added (50 mL). The solution was left to stand for 16 hours at room temperature whereupon impurities were precipitated out of the solution. The precipitate was filtered and the filtrate was collected, evaporated under vacuo and chromatographed on silica gel using chloroform:acetic acid (95:5) to give 6-Maleimidocaproic acid 23 (8 g).

後処理

  1. temperaturethe reaction mixture refluxed for 16 hours
  2. customThe reaction mixture was evaporated under vacuo to an oil and chloroform
  3. additionwas then added (50 mL)
  4. waitThe solution was left
  5. waitto stand for 16 hours at room temperature whereupon impurities
  6. customwere precipitated out of the solution
  7. filtrationThe precipitate was filtered
  8. customthe filtrate was collected
  9. customevaporated under vacuo
  10. customchromatographed on silica gel

出典と根拠

ORDレコード
ord-fdc493cdd95e455b8f79d9c6bd9ce8cf
出典データセット
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06479265B1

反応ノート

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