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The Royal Society of Chemistry"

Olefination of 3-phenyl-1H-indene to Benzofulvene

SyntheticPage 779

Submitted: May 6, 2015, published: May 8, 2015

Authors

Adam Glass (glassac@plu.edu)

Christian Rude (rudeci@plu.edu)

John Fordice (fordicjw@plu.edu)

Katie Caspary (casparke@plu.edu)

Reaction Scheme

Chemicals

3-phenyl-1H-indene (Prepared in House by method of SP696)

3-chlorobenzaldehyde (Oakwood Chemical, 95%)

1,8-Diazabicyclo[5.4.0]undec-7-ene "DBU" (TCI, 98%)

2-MeTHF (Sigma-Aldrich, HPLC grade)

Procedure

The synthesis was performed under ambient atmosphere. To a microwave reaction vial charged with indene  (0.204 g, 1.06 mmol) was added 3-chlorobenzaldehyde (0.154 g, 1.10 mmol), DBU  (0.172 g, 1.13 mmol), and 2-MeTHF (2 mL, 0.53 M). The vial was then heated via variable watt microwave irradiation to 60 °C for 10 minutes with a 30 second pre-stirring period. Upon completion a yellow sheen was observed on the sides of the vial. The reaction mixture was quenched using a silica plug. The solvent was removed under reduced pressure. The crude mixture was purified via preparative chromatography, (90:10 hexane:toluene) yielding the title compound as a crimson red solid, (0.190 g, 58%).

The synthesis was also performed on a 100 mg scale (indene) yielding 90 mg of the title compound (55%). 

Author Comments

3-chlorobenzaldehyde should be added before the DBU, and the time between the addition of the DBU and microwave heating should be minimized in order to maximize yield.

Data

1H NMR (CDCl3, 500 MHz): δ ppm 7.06 (s, 1H), 7.29-7.36 (m, 4H), 7.39-7.44 (m, 2H), 7.46-7.51 (m, 3H), 7.59-7.62 (m, 2H), 7.69-7.75 (m, 3H)

 13C NMR (CDCl3, 125 MHz): δ ppm 119.5, 120.5, 122.5, 125.7, 126.2, 127.60, 127.7, 128.1, 128.2, 128.31,128.6, 129.8, 129.9, 134.6, 135.4, 138.6, 138.8, 140.3, 140.8, 148.3

GC-MS EI [M.+]: Predicted: 314.09, Actual: 314;   Predicted: 315.09 Actual: 315; Predicted: 316.08,  Actual: 3161

Keywords

aldehydes, alkenes, aromatics/arenes

Comments

about starting material and solvent
Very nice reaction. In this reaction author used 3-chloro benzaldehyde is there any specific role for 3-chloro or any other simple aldehyde can do this reaction and another thing about the solvent if we use only THF instead of 2-Me THF is there any effect on reactivity or yield
By Ravindra on June 9, 2015
Response to Ravindra
Most benzaldehydes that we have tried work - though the equivalents of DBU will need to be tuned in some cases. We vary from 1 to 2 equivalents of DBU. THF will generally lower the yield, but still works.
By Adam Glass on June 9, 2015