Реакция #155401

ord-1ec9bc3d671e44158047973099138a77

Уравнение реакции

CCOC(CCCNC(=O)OCC1c2ccccc2-c2ccccc21)OCC
N-Fmoc-4-amino-butyraldehyde diethyl acetal
Cl
HCl
O=CCCCNC(=O)OCC1c2ccccc2-c2ccccc21
N-Fmoc-4-amino-butyraldehyde

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеUpon completion, the organic solvent was removed by rotary evaporation
  2. 2
    Экстракцияthe aqueous layer was extracted with ethyl acetate (2×200 mL)
  3. 3
    ПромывкаThe combined organic layers were washed with 5% NaHCO3 (2×75 mL), brine (75 mL)
  4. 4
    Сушкаdried over Na2SO4
  5. 5
    Фильтрацияfiltered
  6. 6
    Концентрированиеconcentrated to dryness

Методика

To a stirring solution of N-Fmoc-4-amino-butyraldehyde diethyl acetal (0.050 mmol) in 1,4-dioxane (100 mL) was added aq. HCl (100 ml, 1:1 v/v, H2O:conc. HCl) and the reaction progress was monitored by MS. Upon completion, the organic solvent was removed by rotary evaporation, and the aqueous layer was extracted with ethyl acetate (2×200 mL). The combined organic layers were washed with 5% NaHCO3 (2×75 mL), brine (75 mL), dried over Na2SO4, filtered and concentrated to dryness to yield the desired N-Fmoc-4-amino-butyraldehyde (15.35 g, 0.049 mol, 90.0% yield), which was carried through to the next step without further purification: MS m/e [M+Na]+ calcd 332.1. found 332.0.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08822424B2uspto-grants-2014_09