Reaktion #725931
ord-f52a87f6781f4d688bc38fb73f7eb812
Reaktionsgleichung
Benzyloxyacetyl chloride
2-(4-aminophenoxy)propionic acid methyl ester
2-(4-Amino-phenoxy)-propionic acid methyl ester
triethylamine
→
68
Ausbeute 59.8%
2-[4-(2-Benzyloxyacetylamino)phenoxy]propionic acid methyl ester
Ausbeute 59.8%
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1FiltrationSolids were filtered off
- 2workup.DISTILLATIONacetone distilled off
- 3workup.ADDITIONwater (100 ml) added
- 4ExtraktionCrude 68 was extracted into chloroform
- 5Waschenwashed with 5% sodium bicarbonate (2×100 ml), water (200 ml)
- 6Trocknendried over sodium sulphate
- 7workup.DISTILLATIONdistilled
- 8SonstigeCrude 68 was purified by column chromatography on silica gel
Vorschrift
Benzyloxyacetyl chloride (28 g, 152 mmol) was added dropwise to a mixture of 2-(4-aminophenoxy)propionic acid methyl ester 18 (20 g, 102.5 mmol) and triethylamine (23 ml, 165 mmol) in acetone (120 ml) at 0° C. and stirred at room temperature for 12 hrs. Solids were filtered off, acetone distilled off and water (100 ml) added. Crude 68 was extracted into chloroform, washed with 5% sodium bicarbonate (2×100 ml), water (200 ml), dried over sodium sulphate and distilled. Crude 68 was purified by column chromatography on silica gel using benzene as eluant to get pure 68 (21 g, 59.8%) as a light brown powder. M.p: 67-70° C.