Hydrochloric Acid → 1H-Pyrrol-1-ylacetic acid

HRID 1639731

Reaktionsgleichung

Reaktionsgleichung von HRID 1639731
[OH-].[K+].[NH:3]1[CH:7]=[CH:6][CH:5]=[CH:4]1.Br[CH2:9][C:10]([O:12]CC)=[O:11].Cl>O.CS(C)=O>[N:3]1([CH2:9][C:10]([OH:12])=[O:11])[CH:7]=[CH:6][CH:5]=[CH:4]1

Komponenten

7

Versuchsvorschrift

To a mixture of potassium hydroxide (16.7 g) and dry DMSO (150 mL), pyrrole (5 g) was added dropwise at 20-25° C., with stirring under nitrogen atmosphere. Stirring was continued for 1 hr at 20-25° C. Ethyl bromoacetate (24.5 g) was added dropwise at 20-25° C. and stirring was continued for 2 hr. In the reaction mixture (150 mL) DM water was added and pH was made acidic (pH=3) with 20% HCl (50 mL). The reaction mixture was extracted with diethyl ether (2×100 mL). The combined organic extract was washed with DM water (100 mL), saturated brine (100 mL) and dried over Na2SO4. The solvent was evaporated to obtain pyrrol-1-yl-acetic acid.

Aufarbeitung

  1. additionwas added dropwise at 20-25° C.
  2. stirringStirring
  3. stirringstirring
  4. waitwas continued for 2 hr
  5. extractionThe reaction mixture was extracted with diethyl ether (2×100 mL)
  6. extractionThe combined organic extract
  7. washwas washed with DM water (100 mL), saturated brine (100 mL)
  8. dry with materialdried over Na2SO4
  9. customThe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-e2f9c2f5ea444841af1fe7338d03a096
Quelldatensatz
uspto-grants-2012_02
Patentnummer
US08110598B2

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