Реакция #6607

ord-29b56e7bfb744771ab87ed2781bf6d17

Уравнение реакции

O=S(=O)([O-])[O-].[Na+].[Na+]
sodium sulfate
CC(C)[CH2][Al+][CH2]C(C)C.[H-]
diisobutylaluminum hydride
CC1(C)CCC(C)(C)c2cc(OCc3ccc(C#N)cc3)ccc21
4-cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether
O=C(O)C(O)C(O)C(=O)O
tartaric acid
CC1(C)CCC(C)(C)c2cc(OCc3ccc(C=O)cc3)ccc21
title compound
CC1(C)CCC(C)(C)c2cc(OCc3ccc(C=O)cc3)ccc21
4-Formylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether

Растворители

Условия реакции

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

Обработка

  1. 1
    Другоеthe phases were separated
  2. 2
    ЭкстракцияThe aqueous phase was extracted with ether
  3. 3
    Экстракцияthe organic extract
  4. 4
    Промывкаwas washed with saturated tartaric acid solution and water
  5. 5
    Сушкаdried over Na2SO4
  6. 6
    Концентрированиеconcentrated
  7. 7
    ДругоеRecrystallization from reethanol

Методика

15.5 ml (19.7 mmol) of diisobutylaluminum hydride solution (20% in hexane) were added dropwise under nitrogen to a solution of 3 g (9.4 mmol) of 4-cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether in 40 ml of dry ether at 25° C. The mixture was stirred at 25° C. for 40 min and then 250 ml of saturated tartaric acid solution were added dropwise. Subsequently, a little sodium sulfate solution was added, and the phases were separated. The aqueous phase was extracted with ether, and the organic extract was washed with saturated tartaric acid solution and water, dried over Na2SO4 and concentrated. Recrystallization from reethanol resulted in 1.4 g of the title compound of melting point 102°-104° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05248823uspto-grants-1993_09