Hydrochloric Acid → HCID 20318415, Verbindung
Reaktionsgleichung
[C:1]([C:5]1[C:6]([OH:19])=[C:7]([CH3:18])[C:8]([CH3:17])=[C:9]([CH2:11][CH2:12][C:13]([O:15]C)=[O:14])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+].Cl>C(O)C.O>[C:1]([C:5]1[C:6]([OH:19])=[C:7]([CH3:18])[C:8]([CH3:17])=[C:9]([CH2:11][CH2:12][C:13]([OH:15])=[O:14])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2]Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Under nitrogen, a solution of methyl 3-(5-tert.-butyl-2,3-dimethyl-4-hydroxyphenyl)propionate (71.5 g) in 150 ml of ethanol was treated with a solution of 98% sodium hydroxide (12.1 g) in 15 ml of water, and the mixture was heated under reflux for 3 hours. The cold solution was diluted with water to about 1200 ml and then acidified with concentrated hydrochloric acid. The precipitated solid was filtered off and washed with water. Recrystallization from 600 ml of acetonitrile gave the acid, m.p. 191° to 193° C.
Aufarbeitung
- temperaturethe mixture was heated
- temperatureunder reflux for 3 hours
- filtrationThe precipitated solid was filtered off
- washwashed with water
- customRecrystallization from 600 ml of acetonitrile
- customgave the acid, m.p. 191° to 193° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-6028d18beed0491a8c5dd22e7af39eba
- Quelldatensatz
- uspto-grants-1978_07
- Patentnummer
- US04101550
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