Реакция #1161629

ord-6dd39eacc36144babc54687108e4218a

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONto the resulting solution was added, in portions over 45 minutes
  2. 2
    ЭкстракцияThe aqueous mixture was extracted 5 times with diethyl ether
  3. 3
    Промывкаthe combined organic extracts were washed 7 times with 0.2 N hydrochloric acid
  4. 4
    Сушкаtwice with water and once with saturated aqueous sodium chloride solution and dried over magnesium sulfate
  5. 5
    ДругоеThe solvent was evaporated
  6. 6
    Другоеthe resulting crude residue was purified by chromatography on silica gel
  7. 7
    Промывкаeluting with 1:1 ethyl acetate/hexane
  8. 8
    ДругоеThe purified light-yellow oil obtained
  9. 9
    Другоеto crystallize
  10. 10
    ДругоеThe solid which formed
  11. 11
    Другоеwas separated by filtration
  12. 12
    Другоеdried

Методика

To 450 ml of dimethylformamide containing 23.8 ml of triethylamine was added 11.4 g of 2-(4-aminophenyl)-butanol and to the resulting solution was added, in portions over 45 minutes, 21 g of methyl(1,3-dithiolan-2-ylidene)sulfonium iodide. The resulting hazy-yellow solution was stirred for 2 hours and then poured into ice water. The aqueous mixture was extracted 5 times with diethyl ether and the combined organic extracts were washed 7 times with 0.2 N hydrochloric acid, twice with water and once with saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was evaporated and the resulting crude residue was purified by chromatography on silica gel, eluting with 1:1 ethyl acetate/hexane. The purified light-yellow oil obtained was immediately dissolved in warm diethyl ether and allowed to crystallize. The solid which formed was separated by filtration and dried to give 2-[4-(1,3-dithiolan-2-ylideneamino)phenyl]butanol as white spars melting at about 98.5°-100.5° C. This compound has the following structural formula ##STR3##

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04391818uspto-grants-1983_07