Реакция #589047
ord-b6e58a072fec47b98761066fa012a2fa
Уравнение реакции
6-(4-aminophenoxy)-hexanoic acid methyl ester
triethylamine
benzyloxy acetyl chloride
→
53
Выход 22.2%
6-[4-(2-Benzyloxy-acetylamino)-phenoxy]-hexanoic acid methyl ester
Выход 22.2%
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ФильтрацияThe solids were filtered off
- 2workup.DISTILLATIONacetone distilled off
- 3workup.ADDITIONwater (100 ml) added
- 4ЭкстракцияCrude 53 was extracted into chloroform
- 5Промывкаwashed with 5% sodium bicarbonate solution (2×100 ml)
- 6Сушкаwater (100 ml), dried over sodium sulphate
- 7workup.DISTILLATIONdistilled
- 8ДругоеCrude 53 was purified by column chromatography on silica gel
Методика
To a mixture of 6-(4-aminophenoxy)-hexanoic acid methyl ester 17 (25 g, 105 mmol) and triethylamine (21.4 g, 211.6 mmol) in acetone (200 ml) at 0° C. was added dropwise benzyloxy acetyl chloride (25 g, 135.5 mmol) followed by stirring at room temp. for 12 hrs. The solids were filtered off, acetone distilled off and water (100 ml) added. Crude 53 was extracted into chloroform, washed with 5% sodium bicarbonate solution (2×100 ml), then water (100 ml), dried over sodium sulphate and distilled. Crude 53 was purified by column chromatography on silica gel using benzene as eluant to get pure 53 (9 g, 22.2%), an off-white powder with a m.p. between 46-49° C.