Sodium Hydroxide → 2-(3-Bromo-5-chlorophenyl)acetic acid

HRID 1810441Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1810441
C[O:2][C:3](=[O:17])[CH:4]([C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[C:11]([Br:16])[CH:10]=1)C(OC)=O.[OH-].[Na+]>CO>[Br:16][C:11]1[CH:10]=[C:9]([CH2:4][C:3]([OH:17])=[O:2])[CH:14]=[C:13]([Cl:15])[CH:12]=1

Komponenten

4

Versuchsvorschrift

2-(3-Bromo-5-chloro-phenyl)-malonic acid dimethyl ester (19 g, 59 mmol) in MeOH (500 mL) was treated with 1N aqueous NaOH (237 mL, 237 mmol) at 50° C. for 1.5 hours. The mixture was concentrated, and the residue was acidified and extracted twice with EtOAc. The combined organic layers were dried, filtered, and concentrated to give the title compound.

Aufarbeitung

  1. concentrationThe mixture was concentrated
  2. extractionextracted twice with EtOAc
  3. customThe combined organic layers were dried
  4. filtrationfiltered
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-41b759f1484f40c1a41284429219fd41
Quelldatensatz
uspto-grants-2013_01
Patentnummer
US08362044B2

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