Реакция #1051697

ord-8a0e410905f9491b9f33351cd53347d9

Уравнение реакции

CC1(C)CCC(C)(C)c2cc3c(=O)ccoc3cc21
6,6,9,9-tetramethyl-6,7,8,9-tetrahydrobenzo[g]chromen-4-one
CC1(C)CCC(C)(C)c2cc3c(cc21)OCCC3=O
6,6,9,9-tetramethyl-2,3,6,7,8,9-hexahydrobenzo[g]chromen-4-one
Выход 95.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеreaction
  2. 2
    ФильтрацияThe mixture was filtered
  3. 3
    Концентрированиеconcentrated
  4. 4
    Другоеto give a yellow oil
  5. 5
    КонцентрированиеThe oil was passed through a small column of silica (10% EtOAc in hexane) and concentration

Методика

A solution of 6,6,9,9-tetramethyl-6,7,8,9-tetrahydrobenzo[g]chromen-4-one (4.4 g, 17.2 mmol) in 1:1 EtOAc/methanol (250 ml) containing 10% palladium on carbon (1:1 g, 7% by weight) was stirred at room temperature under an atmosphere of hydrogen (balloon) for 14 h. TLC analysis indicated complete reaction. The mixture was filtered and concentrated to give a yellow oil. The oil was passed through a small column of silica (10% EtOAc in hexane) and concentration to give 6,6,9,9-tetramethyl-2,3,6,7,8,9-hexahydrobenzo[g]chromen-4-one (4.2 g, 16.3 mmol, 95%) as a light yellow solid: 1H NMR (400 MHz, CDCl3) δ 7.85 (s, 1H), 6.86 (s, 1H), 4.46 (t, 2H), 2.75 (t, 2H), 1.65 (s, 4H), 1.25 (s, 12H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05770383uspto-grants-1998_06