Реакция #2045048

ord-ca991032d8984228b635676cd4c8fcf6

Уравнение реакции

O=C(Cl)COCc1ccccc1
Benzyloxyacetyl chloride
COC(=O)C(C)Oc1ccc(N)cc1
2-(4-aminophenoxy)propionic acid methyl ester
COC(=O)C(C)Oc1ccc(N)cc1
2-(4-Amino-phenoxy)-propionic acid methyl ester
CCN(CC)CC
triethylamine
COC(=O)C(C)Oc1ccc(NC(=O)COCc2ccccc2)cc1
68
Выход 59.8%
COC(=O)C(C)Oc1ccc(NC(=O)COCc2ccccc2)cc1
2-[4-(2-Benzyloxyacetylamino)phenoxy]propionic acid methyl ester
Выход 59.8%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияSolids were filtered off
  2. 2
    workup.DISTILLATIONacetone distilled off
  3. 3
    workup.ADDITIONwater (100 ml) added
  4. 4
    ЭкстракцияCrude 68 was extracted into chloroform
  5. 5
    Промывкаwashed with 5% sodium bicarbonate (2×100 ml), water (200 ml)
  6. 6
    Сушкаdried over sodium sulphate
  7. 7
    workup.DISTILLATIONdistilled
  8. 8
    ДругоеCrude 68 was purified by column chromatography on silica gel

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08409559B2uspto-grants-2013_04