Reaktion #933786

Reaktionsgleichung

4-amino-5-chloro-2-hydroxybenzoic acid methyl ester

sodium hydride

4-amino-5-chloro-2-hydroxybenzoic acid methyl ester

2-Chloro-N,N-diethylacetamide

→

4-amino-5-chloro-2-[2-(diethylamino)-2-oxoethoxy]benzoic acid methyl ester

Ausbeute 92.0%

Lösungsmittel

dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturA cooled
2. 2
   workup.STIRRINGthe mixture was stirred at 100°-110° C. for 3 hours until gas chromatography
3. 3
   TemperaturThe solution was cooled
4. 4
   Extraktionextracted with ether (3×200 ml)
5. 5
   TrocknenThe combined organic solution was dried (magnesium sulfate)
6. 6
   Einengenconcentrated in vacuo
7. 7
   FiltrationFiltration through alumina (eluted with 3% methanol/methylene chloride) and trituration from petroleum ethers (30°-60°)

Vorschrift

A cooled (0° C.) suspension of 60% sodium hydride/oil dispersion (1.40 g, 0.035 mole) in anhydrous dimethylformamide (60 ml) under nitrogen was treated in portions with 4-amino-5-chloro-2-hydroxybenzoic acid methyl ester (6.05 g, 0.030 mole) and stirred for 30 minutes at room temperature. 2-Chloro-N,N-diethylacetamide (5.40 g, 0.036 mole) was added, and the mixture was stirred at 100°-110° C. for 3 hours until gas chromatography indicated absence of 4-amino-5-chloro-2-hydroxybenzoic acid methyl ester. The solution was cooled and added to ice water (350 ml), then extracted with ether (3×200 ml). The combined organic solution was dried (magnesium sulfate) and concentrated in vacuo. Filtration through alumina (eluted with 3% methanol/methylene chloride) and trituration from petroleum ethers (30°-60°) afforded 8.66 g (92%) of 4-amino-5-chloro-2-[2-(diethylamino)-2-oxoethoxy]benzoic acid methyl ester as a colorless solid; mp 97.5° -99.5° C. (ethyl acetate/hexane).

Quelle