Hydrochloric Acid → DH 990

HRID 596988

Reaktionsgleichung

Reaktionsgleichung von HRID 596988
[C:1]([C:5]1[CH:6]=[C:7]([S:16][CH:17]([CH2:23][CH2:24][CH2:25][CH3:26])[C:18]([O:20]CC)=[O:19])[CH:8]=[C:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:10]=1[OH:11])([CH3:4])([CH3:3])[CH3:2].[OH-].[K+].Cl>C(O)C>[C:12]([C:9]1[CH:8]=[C:7]([S:16][CH:17]([CH2:23][CH2:24][CH2:25][CH3:26])[C:18]([OH:20])=[O:19])[CH:6]=[C:5]([C:1]([CH3:2])([CH3:3])[CH3:4])[C:10]=1[OH:11])([CH3:13])([CH3:14])[CH3:15]

Komponenten

5

Versuchsvorschrift

The ethyl 2-((3,5-di-tert-butyl-4-hydroxyphenyl)thio)hexanoate product (75 grams; 0.195 mole) obtained in Example 2 was dispersed in 300 ml. of 95% ethanol and 500 ml. of 5N potassium hydroxide added thereto. The resulting reaction mixture was heated on a steam bath at the boiling point under gentle reflux for about 90 minutes with occasional stirring. Following the heating period, the reaction mixture was poured into 2000 ml. of 5% HCl with vigorous stirring. The white precipitate formed upon acidification was obtained by filtration and washed with water. Recrystallization (twice) of the precipitate from a methylene chloride-hexane mixture gave the desired 2-((3,5-di-tert-butyl-4-hydroxyphenyl)thio)hexanoic acid compound having a melting point of 140°-142° C.

Aufarbeitung

  1. additionwas dispersed in 300 ml
  2. customThe resulting reaction mixture
  3. temperaturewas heated on a steam bath at the boiling point
  4. temperatureunder gentle reflux for about 90 minutes with occasional stirring
  5. additionthe reaction mixture was poured into 2000 ml
  6. customThe white precipitate formed upon acidification
  7. customwas obtained by filtration
  8. washwashed with water
  9. customRecrystallization (twice) of the precipitate from a methylene chloride-hexane mixture

Quellen und Nachweise

ORD-Eintrag
ord-94e928ef751f4e1b8c9007a4846a1d4e
Quelldatensatz
uspto-grants-1977_03
Patentnummer
US04012523

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