Реакция #725953

ord-d8e9f96e586443b7bc5a64069ecb63f1

Уравнение реакции

O=Cc1ccc(O)c(O)c1
3,4-Dihydroxybenzaldehyde
O=C([O-])[O-].[Cs+].[Cs+]
Cesium carbonate
CCCCC/C=C\C/C=C\CCCCCCCCOS(C)(=O)=O
Linoleyl mesylate
CCCCC/C=C\C/C=C\CCCCCCCCc1cccc(C=O)c1CCCCCCCC/C=C\C/C=C\CCCCC
brown oil
Выход 98.7%
CCCCC/C=C\C/C=C\CCCCCCCCc1cccc(C=O)c1CCCCCCCC/C=C\C/C=C\CCCCC
Dilinoleylbenzaldehyde
Выход 98.7%

Реагенты

Нет

Растворители

Условия реакции

Температура
100°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеsealed
  2. 2
    Другоеflushed with argon
  3. 3
    ТемператураThe reaction mixture was cooled to room temperature
  4. 4
    Фильтрацияfiltered
  5. 5
    ПромывкаThe solids were washed with 1,2-dichloroethane
  6. 6
    КонцентрированиеThe combined filtrate and washes were concentrated
  7. 7
    Другоеdried under high vacuum at 65° C.
  8. 8
    Другоеto remove residual diglyme
  9. 9
    ДругоеThe resultant yellow oil was purified via flash chromatography (5% ethyl acetate in hexanes)

Методика

3,4-Dihydroxybenzaldehyde (2.76 g, 20.0 mmol) was weighed into a 200 mL round bottomed flask with a stir bar. The flask was charged with diglyme (100 mL), septum sealed and flushed with argon. Cesium carbonate (19.5 g, 60.0 mmol) was added to the solution slowly in portions. Linoleyl mesylate (15.2 g, 44.0 mmol) was added via syringe. The reaction mixture was heated to 100° C. under slight positive pressure of argon. The reaction mixture was cooled to room temperature and filtered. The solids were washed with 1,2-dichloroethane. The combined filtrate and washes were concentrated and then dried under high vacuum at 65° C. to remove residual diglyme. The resultant yellow oil was purified via flash chromatography (5% ethyl acetate in hexanes) to afford 11.9 g (94%) of a brown oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07691405B2uspto-grants-2010_04