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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Ethanol → 2-Imidazoline, 4,4-dimethyl-1-isopropyl-2-undecyl-

HRID 2352207
ノート
印刷プレビュー

反応式

HRID 2352207 の反応式
[C:1](OCC)(=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH:17]([NH:20][CH2:21][C:22]([CH3:25])([NH2:24])[CH3:23])([CH3:19])[CH3:18].C(O)C>>[CH3:23][C:22]1([CH3:25])[CH2:21][N:20]([CH:17]([CH3:19])[CH3:18])[C:1]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])=[N:24]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 3

HCID 702EthanolHCID 7800Ethyl DodecanoateHCID 795322-Amino-1,1-dimethylethylisopropylamine

生成物 1

HCID 528882-Imidazoline, 4,4-dimethyl-1-isopropyl-2-undecyl-収率 58%

実験手順

22.84 g. (100 mmoles) of ethyl laurate and 15.34 g. (118 mmoles) of Nl -isopropyl-2-methyl-1,2-propanediamine is heated at 130°-230° C. until approximately 100 mmoles of ethanol is collected. Toluene is then cautiously added and the heating is continued until no more water separates. The solution is acidified, the aqueous layer is separated and basified with NaOH. This is extracted with ethyl acetate, the organic extract is dried and concentrated. The oil is distilled at 150-152° C./1.2 mm to give 16.74 g (58%) of product.

後処理

  1. customis collected
  2. additionToluene is then cautiously added
  3. customthe aqueous layer is separated
  4. extractionThis is extracted with ethyl acetate
  5. extractionthe organic extract
  6. customis dried
  7. concentrationconcentrated
  8. distillationThe oil is distilled at 150-152° C./1.2 mm

出典と根拠

ORDレコード
ord-03348d401ea941e6834472e6d24f6bd9
出典データセット
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04876249

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート