Hydrochloric Acid → Methyl 4-tetradecanoylpyrrole-2-carboxylate

HRID 129336

Reaktionsgleichung

Reaktionsgleichung von HRID 129336
[NH:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([O:8][CH3:9])=[O:7].[C:10](Cl)(=[O:24])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].Cl>C1C=CC=CC=1>[CH3:9][O:8][C:6]([C:2]1[NH:1][CH:5]=[C:4]([C:10](=[O:24])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[CH:3]=1)=[O:7]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 66986Myristoyl chlorideHCID 136930Methyl pyrrole-2-carboxylate

Produkt 1

HCID 15023256Methyl 4-tetradecanoylpyrrole-2-carboxylateAusbeute 54 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

To a solution (5 ml) of 1.25 g (10 mmol) of methyl pyrrole -2-carboxylate in benzene was added 2.71 g (11 mmol) of tetradecanoyl chloride under ice-cooling, followed by adding 1.73 ml) (15 mmol) of stannic chloride dropwise thereto. The mixture was stirred for 2 hours at room temperature, treated with diluted hydrochloric acid and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. After removing the solvent under reduced pressure, the product was purified by subjecting it to column chromatography over silica gel (ethyl acetate/hexane=1/7) to obtain 1.80 g (54% yield) of methyl-4-tetradecanoylpyrrole-2-carboxylate.

Aufarbeitung

  1. temperaturecooling
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customAfter removing the solvent under reduced pressure
  6. customthe product was purified

Quellen und Nachweise

ORD-Eintrag
ord-201e210710864e87ae66284481e3a106
Quelldatensatz
uspto-grants-1995_11
Patentnummer
USRE035096

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