Реакция #2507828

ord-63485a51519049168b72d9ac649dbebd

Уравнение реакции

O=CN1CCCCC1
N-formylpiperidine
[Li][CH2]CCC
n-butyllithium
CCCCCC1COc2cc(Br)c(F)cc2C1
7-bromo-6-fluoro-3-pentylchroman
Cl
hydrochloric acid
CCCCCC1COc2cc(C=O)c(F)cc2C1
6-fluoro-3-pentylchroman-7-carbaldehyde

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted three times with MTB ether
  2. 2
    Промывкаphases are washed with water and sat. sodium chloride soln
  3. 3
    Сушкаand dried over sodium sulfate
  4. 4
    Другоеthe solvent is removed in vacuo
  5. 5
    Другоеthe residue is recrystallised from heptane at −25° C.

Методика

15.5 g (51.5 mmol) of 7-bromo-6-fluoro-3-pentylchroman are dissolved in 85 ml of THF, and 35 ml (55.7 mmol) of a 15 percent solution of n-butyllithium in n-hexane are slowly added at −70° C. After 1 h, 6.3 ml (56.7 mmol) of N-formylpiperidine in 15 ml of THF are added dropwise, and the mixture is stirred for 1 h. The batch is subsequently allowed to thaw, added to water, acidified using dil. hydrochloric acid and extracted three times with MTB ether. The combined org. phases are washed with water and sat. sodium chloride soln. and dried over sodium sulfate, the solvent is removed in vacuo, and the residue is recrystallised from heptane at −25° C., giving 6-fluoro-3-pentylchroman-7-carbaldehyde as colourless crystals (Rf=0.4; 1-chlorobutane).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07955664B2uspto-grants-2011_06