Реакция #1960507
ord-cb272f2a154641a290b0f320701a0725
Уравнение реакции
7-ethoxy-1,2-difluoro-3-[1-(4-propylcyclohexyl)prop-2-ynyloxy]naphthalene
→
8-ethoxy-5,6-difluoro-3-(4-propylcyclohexyl)-3H-benzo[f]chromene
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Промывкаwashed a number of times with hydrochloric acid
- 2ДругоеThe organic phase is dried
- 3Другоеevaporated to dryness
- 4ДругоеThe residue is purified by column chromatography (SiO2, n-heptane:MTBE=4:1)
- 5ДругоеThe further purification
- 6Другоеis carried out by recrystallisation from n-heptane
Методика
7.75 g (about 18.6 mmol) of 7-ethoxy-1,2-difluoro-3-[1-(4-propylcyclohexyl)prop-2-ynyloxy]naphthalene are heated at 205° C. for 4.5 h in 80 ml of N,N-diethylaniline. The batch is diluted with MTBE and washed a number of times with hydrochloric acid. The organic phase is dried using sodium sulfate and evaporated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:MTBE=4:1). The further purification is carried out by recrystallisation from n-heptane, giving 8-ethoxy-5,6-difluoro-3-(4-propylcyclohexyl)-3H-benzo[f]chromene as a yellow solid.