Reaction #2195479

ord-058ade992a7847fab02388fcad821b28

Reaction equation

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

Solvents

Conditions

Temperature
100°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Othersealed
  2. 2
    Otherflushed with argon
  3. 3
    TemperatureThe reaction mixture was cooled to room temperature
  4. 4
    Filtrationfiltered
  5. 5
    WashThe solids were washed with 1,2-dichloroethane
  6. 6
    ConcentrationThe combined filtrate and washes were concentrated
  7. 7
    Otherdried under high vacuum at 65° C.
  8. 8
    Otherto remove residual diglyme
  9. 9
    OtherThe resultant yellow oil was purified via flash chromatography (5% ethyl acetate in hexanes)

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07514099B2uspto-grants-2009_04