Sodium Hydroxide → 2-Butyloctanoic acid

HRID 1525627Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1525627
[CH2:1]([C:5](CCCC)([C:14]([OH:16])=[O:15])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])[CH2:2][CH2:3][CH3:4].[OH-].[Na+]>>[CH2:1]([CH:5]([C:14]([OH:16])=[O:15])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])[CH2:2][CH2:3][CH3:4]

Komponenten

3

Versuchsvorschrift

The above chiral salt, an organic solvent, an alkaline aqueous medium, and dibutyl 1,6-dicarboxy-hexane are mixed in a vessel. 1.0 equivalents (based upon the moles and equivalents of dibutyl 1,6-dicarboxy-hexane) of alkalizing agent, such as sodium hydroxide, is added, optionally with heating. The hydrolysis is allowed to proceed to completion. The mono-esterified butyl 1,6-dicarboxy-hexane is contained within the aqueous phase. The phases are separated. The aqueous phase is acidified with dilute acid to pH 4.5 with cooling. The butyl 1,6-dicarboxy-hexane is isolated by filtration or extraction with diethyl ether.

Aufarbeitung

  1. temperatureoptionally with heating
  2. customThe phases are separated
  3. additionwith dilute acid to pH 4.5
  4. temperaturewith cooling

Quellen und Nachweise

ORD-Eintrag
ord-c90fac2c5380448eb09d6b87dd63e126
Quelldatensatz
uspto-grants-2015_07
Patentnummer
US09085525B2

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