Реакция #1051685

ord-5807c4c9cc34484db11ca01c6d66fa1d

Уравнение реакции

O=C(CO)c1ccccc1
hydroxyacetophenone
C1CCNC1
pyrrolidine
CC(C)=O
acetone
Cc1ccc(S(=O)(=O)O)cc1
p-TsOH
CC1(C)CC(=O)c2cc3c(cc2O1)C(C)(C)CCC3(C)C
2,3,6,7,8,9-hexahydro-2,2,6,6,9,9-hexamethylbenzo [g]chromen-4-one
Выход 26.0%

Реагенты

Нет

Растворители

Условия реакции

Температура
25°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураat reflux for 48 hours
  2. 2
    ЭкстракцияAqueous work up (Et2O extraction)
  3. 3
    Другоеgave a yellowish brown solid
  4. 4
    ДругоеRecrystallization from hexane

Методика

A solution of the above hydroxyacetophenone (1.86 g, 7.5 mmol), pyrrolidine (590 mg, 7.5 mmol), acetone (850 mg, 14.6 mmol), and a catalytic amount of p-TsOH in benzene (650 ml) was heated at reflux for 48 hours. The mixture was cooled to 25° C. and diluted with 1N HCl (35 ml). Aqueous work up (Et2O extraction) gave a yellowish brown solid. Recrystallization from hexane afforded 2,3,6,7,8,9-hexahydro-2,2,6,6,9,9-hexamethylbenzo [g]chromen-4-one (structure 1) as fine white crystals (560 mg, 1.95 mmol, 26%): 1H NMR (400 MHz, CDCl3) δ 7.3 (s, 1H), 6.85 (s, 1H), 2.68 (s, 2H), 1.68 (s, 4H), 1.45 (s, 6H), 1.26 (s, 12H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05770382uspto-grants-1998_06