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Diethylenetriamine → 9-Decyl-1,4,7-triazecane-8,10-dione

HRID 2255349
ノート
印刷プレビュー

反応式

HRID 2255349 の反応式
[CH2:1]([CH:11]([C:17]([O-:19])=O)[C:12]([O:14]CC)=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[NH2:20][CH2:21][CH2:22][NH:23][CH2:24][CH2:25][NH2:26]>C(O)C>[CH2:1]([CH:11]1[C:12](=[O:14])[NH:26][CH2:25][CH2:24][NH:23][CH2:22][CH2:21][NH:20][C:17]1=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]
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 8111DiethylenetriamineHCID 19798168HCID 19798168、化合物

生成物 1

HCID 197981679-Decyl-1,4,7-triazecane-8,10-dione収率 62.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A one litter round bottomed flask was charged with 0.076 mol (22.80 g) of ethyl α-decylmalonate (from above), 0.076 mol (7.74 g) diethylene triamine and 500 ml absolute ethanol. The mixture was refluxed for 42 days. During this period two ml aliquotes of solution were removed by hyperdermic syringe on days 7,15,22, and 37 for NMR analysis to determine the completeness of the reaction. After termination of the reflux, the ethanol was removed under reduced pressure and the product recrystallized from cold acetonitrile to yield 14.71 grams of a white heavy precipitate representing approximately a 62.1% conversion and having NMR characterizations in CDCL3, with signals reported in ppm downfield relative to TMS:

後処理

  1. temperatureThe mixture was refluxed for 42 days
  2. waitDuring this period two ml aliquotes of solution
  3. customwere removed by hyperdermic syringe on days 7,15,22, and 37 for NMR analysis
  4. customthe completeness of the reaction
  5. customAfter termination of the reflux, the ethanol was removed under reduced pressure
  6. customthe product recrystallized from cold acetonitrile

出典と根拠

ORDレコード
ord-c445c65733934b8ea137a6c022b56db3
出典データセット
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05240573

反応ノート

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