Reacción #2075687

ord-73633add99d24741aaee19eb74ab83ca

Ecuación de reacción

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
Rendimiento 98.7%
CCCCC/C=C\C/C=C\CCCCCCCCc1cccc(C=O)c1CCCCCCCC/C=C\C/C=C\CCCCC
Dilinoleylbenzaldehyde
Rendimiento 98.7%

Disolventes

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrosealed
  2. 2
    Otroflushed with argon
  3. 3
    TemperaturaThe reaction mixture was cooled to room temperature
  4. 4
    Filtraciónfiltered
  5. 5
    LavadoThe solids were washed with 1,2-dichloroethane
  6. 6
    ConcentraciónThe combined filtrate and washes were concentrated
  7. 7
    Otrodried under high vacuum at 65° C.
  8. 8
    Otroto remove residual diglyme
  9. 9
    OtroThe resultant yellow oil was purified via flash chromatography (5% ethyl acetate in hexanes)

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07641915B2uspto-grants-2010_01