تفاعل #6607

ord-29b56e7bfb744771ab87ed2781bf6d17

معادلة التفاعل

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

المذيبات

ظروف التفاعل

درجة الحرارة
25°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe phases were separated
  2. 2
    استخلاصThe aqueous phase was extracted with ether
  3. 3
    استخلاصthe organic extract
  4. 4
    غسيلwas washed with saturated tartaric acid solution and water
  5. 5
    تجفيفdried over Na2SO4
  6. 6
    تركيزconcentrated
  7. 7
    أخرىRecrystallization from reethanol

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05248823uspto-grants-1993_09