Реакция #348434

ord-43b331fd1f9b45f1a0082618cdad1ce9

Уравнение реакции

CC1(CBr)S[C@@H]2C(NC(=O)Cc3ccccc3)C(=O)N2C1C(=O)OCC(Cl)(Cl)Cl
2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)-penam-3-carboxylate
CO
methanol
COCC1(C)S[C@@H]2C(NC(=O)Cc3ccccc3)C(=O)N2C1C(=O)OCC(Cl)(Cl)Cl
2,2,2-trichloroethyl 2-methoxymethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate

Растворители

Условия реакции

Температура
-10°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe mixture was stirred for 2 hours at the same temperature
  2. 2
    Фильтрацияthe reaction mixture was filtered
  3. 3
    Промывкаthe filtrate was washed with sodium bicarbonate aqueous solution
  4. 4
    Сушкаwith water, dried over magnesium sulfate
  5. 5
    Концентрированиеconcentrated
  6. 6
    Промывкаeluted with chloroform
  7. 7
    ДругоеThe eluate was separated into fractions of about 20 ml
  8. 8
    Другоеthe first and second fractions were collected
  9. 9
    workup.DISTILLATIONAfter distilling off the solvent
  10. 10
    Другоеthe residue was dried

Методика

2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)-penam-3-carboxylate (1.10 g) was dissolved in methylene chloride (12 ml) and to this solution was added methanol (3 ml). And to the solution was added silver fluoroborate (0.45 g) under stirring under cooling at -10° C. and the mixture was stirred for 2 hours at the same temperature. After the reaction was completed, the reaction mixture was filtered and the filtrate was washed with sodium bicarbonate aqueous solution and then with water, dried over magnesium sulfate and thereafter concentrated. The residue was subjected to column chromatography on silica gel (25 g) and eluted with chloroform. The eluate was separated into fractions of about 20 ml and the first and second fractions were collected. After distilling off the solvent, the residue was dried to give oily 2,2,2-trichloroethyl 2-methoxymethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04164497uspto-grants-1979_08