Sodium Hydroxide → HCID 12897098, Verbindung

HRID 1981030Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1981030
[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([O:6][C:7]2[CH:8]=[C:9]([C:12]([O:14]CCO)=[O:13])[NH:10][CH:11]=2)=[CH:4][CH:3]=1.[OH-].[Na+]>CC(C)=O>[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([O:6][C:7]2[CH:8]=[C:9]([C:12]([OH:14])=[O:13])[NH:10][CH:11]=2)=[CH:4][CH:3]=1

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 20400896HCID 20400896, Verbindung

Produkt 1

HCID 12897098HCID 12897098, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

2-Hydroxyethyl 4-(4-chlorophenoxy)pyrrole-2-carboxylate (400 mg.) was dissolved in 10 ml. of acetone and 10 ml. of 1N sodium hydroxide and left to stand at room temperature for approximately 16 hours. Acetone was evaporated in vacuo, the aqueous residue was acidified with conc. hydrochloric acid and crystalline product (320 mg.) recovered by filtration. Recrystallization from ether/hexane of 400 mg. of product prepared in this manner afforded purified 4-(4-chlorophenoxy)pyrrole-2-carboxylic acid (234 mg., m.p. 188°-190° C., m/e 237).

Aufarbeitung

  1. customAcetone was evaporated in vacuo
  2. filtrationrecovered by filtration
  3. customRecrystallization from ether/hexane of 400 mg
  4. customof product prepared in this manner
  5. customafforded
  6. custompurified 4-(4-chlorophenoxy)pyrrole-2-carboxylic acid (234 mg., m.p. 188°-190° C., m/e 237)

Quellen und Nachweise

ORD-Eintrag
ord-81d9af303243478fb5edb6e1aab68f61
Quelldatensatz
uspto-grants-1985_04
Patentnummer
US04511576

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