Reaction #725909
ord-1aa2e1a9f49c4854887043def0f25d47
Reaction equation
6-[4-(2-Hydroxyethoxycarbonylamino)phenoxy]hexanoic acid methyl ester
6-[4-(2-Hydroxy-ethoxycarbonylamino)-phenoxy]-hexanoic acid methyl ester
6-(4-Isocyanatophenoxy) hexanoic acid methyl ester
6-(4-Isocyanato-phenoxy)-hexanoic acid methyl ester
→
38
Yield 95.0%
6-(4-{2-[4-(5-Methoxycarbonyl-pentyloxy)-phenylcarbamoyloxy]-ethoxycarbonylamino}-phenoxy)-hexanoic acid methyl ester
Yield 95.0%
Reactants
Reagents
None
Solvents
Conditions
Temperature
60°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1workup.DISTILLATIONToluene was distilled off
- 2workup.ADDITIONwater (50 ml) was added
- 3FiltrationThe solid was filtered
- 4Otherdried
- 5Otherto give crude 38, which
- 6Otherwas purified by column chromatography on silica gel
Procedure
To a mixture of 6-[4-(2-Hydroxyethoxycarbonylamino)phenoxy]hexanoic acid methyl ester 37 (5 g, 15.38 mmol) in toluene (50 ml) was added 6-(4-Isocyanatophenoxy) hexanoic acid methyl ester 36 (4 g, 15.2 mmol) at room temperature and heated to 60° C. for 2 hours. Toluene was distilled off and water (50 ml) was added. The solid was filtered and dried to give crude 38, which was purified by column chromatography on silica gel using chloroform as eluant to get pure 38 (8.5 g, 94%) as a white powder. M.p: 118-120.5° C.