Isoamylamine → Hexane

HRID 2227145

反応式

HRID 2227145 の反応式
[CH2:1]([NH2:6])[CH2:2][CH:3]([CH3:5])[CH3:4].[C:7]([O:17]CC)(=O)[CH:8]([CH2:10][C:11]([O:13]CC)=O)[OH:9]>>[CH2:1]([NH:6][C:7](=[O:17])[CH:8]([CH2:10][C:11]([NH:6][CH2:1][CH2:2][CH:3]([CH3:5])[CH3:4])=[O:13])[OH:9])[CH2:2][CH:3]([CH3:5])[CH3:4].[CH3:7][CH2:8][CH2:1][CH2:2][CH2:3][CH3:5]

参加物

4

実験手順

N,N′-Di-iso-pentyl DL-malamide was prepared by the reaction of iso-pentylamine with diethyl DL-malate. To a round-bottomed flask were added diethyl DL-malate (20.013 g, 0.1052 mole, 1 eq) and iso-pentylamine (27.778 g, 3.03 eq). The clear light yellow solution was stirred for 20 hours at room temperature prior to the removal of the excess amine under vacuum with heating. A white waxy solid was obtained. The solid was triturated with hexane (4×100 mL); and the product was filtered through a glass frit after each trituration. Finally, the material was transferred to a round-bottomed flask and the white solid was dried under vacuum for one hour while heating (<100° C.) to remove any residual amine and hexane (28.99 g, ˜100% yield). The product was ˜100% pure as determined by NMR analyses.

後処理

  1. customto the removal of the excess amine under vacuum
  2. temperaturewith heating
  3. customA white waxy solid was obtained
  4. customThe solid was triturated with hexane (4×100 mL)
  5. filtrationand the product was filtered through a glass frit after each trituration
  6. customFinally, the material was transferred to a round-bottomed flask
  7. customthe white solid was dried under vacuum for one hour
  8. temperaturewhile heating (<100° C.)

出典と根拠

ORDレコード
ord-8d37c69e214c4467ba5e64bcae19322b
出典データセット
uspto-grants-2002_07
特許番号
US06413914B1

関連ノート

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