Реакция #1797474

ord-2c2ab0d5068145fab61027f230fe51d0

Уравнение реакции

[O]=[Cr](=[O])([O-])[Cl].c1cc[nH+]cc1
PCC
OCCCCCCOCc1ccccc1
6-benzyloxy-1-hexanol
O=CCCCCCOCc1ccccc1
6-benzyloxy-1-hexanal

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияfiltered through 50 g of silica gel
  2. 2
    ДругоеThe solvent was removed
  3. 3
    Другоеthe crude oil was separated chromatographically on silica gel using
  4. 4
    workup.ADDITIONa mixture of hexane

Методика

Synthesis of [18F]-FCPHA was performed using the following method. PCC (pyridinium chlorochromate; 24.8 g, 115.2 mmol) was slowly added in portions to a solution of 6-benzyloxy-1-hexanol (20 g, 96 mmol) in 200 ml of methylene chloride at room temperature (25° C., RT). The black mixture was stirred for 2 hours, and filtered through 50 g of silica gel. The solvent was removed and the crude oil was separated chromatographically on silica gel using a mixture of hexane:ethyl acetate at a ratio of 90:10. This yielded the aldehyde equivalent, 6-benzyloxy-1-hexanal, at a scale of 14 g (70%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07790142B2uspto-grants-2010_09