Reaktion #9721

ord-55f2e447a6be46f59025fb20b44ca092

Reaktionsgleichung

Cl
hydrochloric acid
CCOC(=O)COc1ccc(OC(C)=O)cc1C
ethyl[4-(acetyloxy)-2-methylphenoxy]acetate
CCOC(=O)COc1ccc(OC(C)=O)cc1C
intermediate 6
CCOC(=O)COc1ccc(OC(C)=O)cc1C
ethyl[4-(acetyloxy)-2-methylphenoxy]acetate
CC[O-].[Na+]
sodium ethoxide
CCOC(=O)COc1ccc(O)cc1C
solution
CCOC(=O)COc1ccc(O)cc1C
ethyl(4-hydroxy-2-methylphenoxy)acetate

Lösungsmittel

Reaktionsbedingungen

Temperatur
45°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture as cooled to 22° C.

Vorschrift

A solution of ethyl[4-(acetyloxy)-2-methylphenoxy]acetate (intermediate 6, 148 g) in ethanol (1300 ml) was treated with sodium ethoxide (41.3 g) and the mixture heated to 45° C. for 2.5 hours. The mixture as cooled to 22° C. and concentrated hydrochloric acid added to give a neutral (pH 7) solution. The resulting mixture was concentrated and the residue dissolved in a mixture of t-butylmethyl ether, water and brine. The organic layer was separated, washed with brine and dried over sodium sulfate and filtered. The filtrate was concentrated to give a brown solid which was further purified by precipitation from a solution in dichloromethane (100 ml) on addition of cyclohexane (710 ml) to give the title compound as a brown solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091237B2uspto-grants-2006_08