Реакция #58450

ord-833207da9f374c3c903eabc45f79e847

Уравнение реакции

[K+].[OH-]
potassium hydroxide
CC(C)(C)OC(=O)N1CCCCC1C(=O)c1ccc(-c2ccc(F)cc2)o1
(RS)-1-(tert-butyloxycarbonyl)-2-((5-(4-fluorophenyl)-furan-2-yl)carbonyl)piperidine
NN.O
hydrazine hydrate
O
water
Fc1ccc(-c2ccc(CC3CCCCN3)o2)cc1
title compound
Выход 63.3%
Fc1ccc(-c2ccc(CC3CCCCN3)o2)cc1
(RS)-2-(5-(4-Fluorophenyl)-furan-2-ylmethyl)-piperidine
Выход 63.3%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe mixture heated at 200° C. for 18 h
  2. 2
    Экстракцияextracted with diethyl ether (3×75 ml)
  3. 3
    СушкаThe combined organic extracts were dried (Na2SO4)
  4. 4
    Другоеevaporated in vacuo

Методика

To a solution of (RS)-1-(tert-butyloxycarbonyl)-2-((5-(4-fluorophenyl)-furan-2-yl)carbonyl)piperidine (2.0 g, 5.36 mmol) in diethylene glycol (20 g), was added hydrazine hydrate (0.31 ml, 5.36 mmol) and the resultant mixture heated at 100° C. for 30 min. After cooling to room temperature, potassium hydroxide (1.0 g, 17.8 mmol) was added and the mixture heated at 200° C. for 18 h. The reaction mixture was then poured into water (100 ml) and extracted with diethyl ether (3×75 ml). The combined organic extracts were dried (Na2SO4) and evaporated in vacuo to give the title compound as a brown oil (0.88 g, 63%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07423052B2uspto-grants-2008_09