Réaction #2075687

ord-73633add99d24741aaee19eb74ab83ca

Équation de réaction

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

Solvants

Conditions de réaction

Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.v1Brevet: US07641915B2uspto-grants-2010_01