Réaction #725903
ord-79436a047415479ca8505657f7179884
Équation de réaction
[4-(2-Hydroxy-ethoxycarbonylamino)-phenoxy]-acetic acid methyl ester
(4-Isocyanato-phenoxy)-acetic acid methyl ester
→
30
Rendement 56.5%
{4-[2-(4-Methoxycarbonylmethoxy-phenylcarbamoyloxy)-ethoxycarbonylamino]-phenoxy}-acetic acid methyl ester
Rendement 56.5%
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Température
50°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1workup.DISTILLATIONToluene was distilled off
- 2workup.ADDITIONwater (10 ml) was added
- 3ExtractionCrude 30 was extracted into chloroform
- 4Séchagedried over sodium sulphate
- 5workup.DISTILLATIONdistilled
- 6Autrepurified by column chromatography on silica gel
Mode opératoire
To [4-(2-Hydroxy-ethoxycarbonylamino)-phenoxy]-acetic acid methyl ester 29 (1 g, 3.72 mmol) in toluene (10 ml) was added (4-Isocyanato-phenoxy)-acetic acid methyl ester 28 (0.8 g, 3.8 mmol) at room temperature and heated to 50° C. for 20 hours. Toluene was distilled off and water (10 ml) was added. Crude 30 was extracted into chloroform, dried over sodium sulphate, distilled and purified by column chromatography on silica gel using chloroform as eluant to get pure 30 (1 g, 56.5%) as a white fluffy powder.