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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → 2-Imidazoline, 4,4-dimethyl-1-isopropyl-2-undecyl-

HRID 2352207
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HRID 2352207 반응식
[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
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참가 물질

4

반응물 3

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

생성물 1

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

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-03348d401ea941e6834472e6d24f6bd9
출처 데이터셋
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04876249

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