Réaction #725933
ord-bd4081c1094c4584837a87fa6f2920d5
Équation de réaction
Benzyloxyacetyl chloride
6-(4-aminophenoxy)hexanoic acid methyl ester
6-(4-Amino-phenoxy)-hexanoic acid methyl ester
triethylamine
→
70
Rendement 22.2%
6-[4-(2-Benzyloxyacetylamino)phenoxy]hexanoic acid methyl ester
Rendement 22.2%
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1FiltrationSolids were filtered off
- 2workup.DISTILLATIONacetone distilled off
- 3workup.ADDITIONwater (100 ml) added
- 4ExtractionCrude 70 was extracted into chloroform
- 5Lavagewashed with 5% sodium bicarbonate solution (2×100 ml), water (100 ml)
- 6Séchagedried over sodium sulphate
- 7workup.DISTILLATIONdistilled
- 8AutreCrude 70 was purified by column chromatography on silica gel
Mode opératoire
Benzyloxyacetyl chloride (25 gm, 135.5 mmol) was added dropwise to a mixture of 6-(4-aminophenoxy)hexanoic acid methyl ester 21 (25 g, 105 mmol) and triethylamine (21.4 g, 211.6 mmol) in acetone (200 ml) at 0° C. and stirred at room temp. for 12 hrs. Solids were filtered off, acetone distilled off and water (100 ml) added. Crude 70 was extracted into chloroform, washed with 5% sodium bicarbonate solution (2×100 ml), water (100 ml), dried over sodium sulphate and distilled. Crude 70 was purified by column chromatography on silica gel using benzene as eluant to get pure 70 (9 g, 22.2%) as a off-white powder. M.p: 46-49° C.