Stearic Acid → 1H-Indole-2-carboxylic acid, 3-(1-oxododecyl)-, ethyl ester

HRID 382827Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 382827
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([O:12][CH2:13][CH3:14])=[O:11].[C:15](O)(=[O:33])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]CCCCCC.FC(F)(F)C(OC(=O)C(F)(F)F)=O.[OH-].[Na+]>C(Cl)Cl>[C:15]([C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][C:2]=1[C:10]([O:12][CH2:13][CH3:14])=[O:11])(=[O:33])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]

Komponenten

6

Versuchsvorschrift

A mixture of 3.8 g (20 mmol) of ethyl indole-2-carboxylate, 6.0 g (30 mmol) of octadecanoic acid, 1.0 g of polyphosphoric acid, 20 ml of absol. CH2Cl2 and 4.4 ml of trifluoroacetic anhydride is stirred at room temperature for 4 h. Then 1 M NaOH is added, and the mixture is extracted with ether. The ether phase is dried over Na2SO4 and the solvent is distilled off. The product precipitates after addition of petroleum ether.

Aufarbeitung

  1. extractionthe mixture is extracted with ether
  2. dry with materialThe ether phase is dried over Na2SO4
  3. distillationthe solvent is distilled off
  4. customThe product precipitates
  5. additionafter addition of petroleum ether

Quellen und Nachweise

ORD-Eintrag
ord-0563c47bc0a54358ac6a36e284a2ab80
Quelldatensatz
uspto-grants-2001_10
Patentnummer
US06310217B1

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