| Identification | Back Directory | [Name]
2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde | [CAS]
33985-71-6 | [Synonyms]
9-Formyljulolidine
2,3,6,7-Tetrahydro-1
9-Julolidinecarboxaldehyde
9-Julolidinecarboxaldehyde>
1,2,3,4,5,6-Hexahydro-3a-aza-3aH-phenalene-8-carbaldehyde
2,3,3a,4,5,6-Hexahydro-3a-aza-1H-phenalene-8-carbaldehyde
2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine-9-carbaldehyde
1,2,3,5,6,7-Hexahydropyrido[3,2,1-ij]quinoline-9-carbaldehyde
5H-BENZO(IJ)QUINOLIZINE-9-CARBOXALDEHYDE, 2,3,6,7-TETRAHYDRO-1
2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde
1H,5H-Benzo[ij]quinolizine-9-carboxaldehyde, 2,3,6,7-tetrahydro-
2,3,6,7-Tetrahydro-1H,5H-pyrido-[3,2,1-ij]quinoline-9-carbaldehyde | [Molecular Formula]
C13H15NO | [MDL Number]
MFCD00151555 | [MOL File]
33985-71-6.mol | [Molecular Weight]
201.264 |
| Chemical Properties | Back Directory | [Melting point ]
83 °C | [Boiling point ]
404.8±44.0 °C(Predicted) | [density ]
1.18±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,2-8°C | [solubility ]
soluble in Methanol | [form ]
powder to crystal | [pka]
3.15±0.20(Predicted) | [color ]
Light orange to Yellow to Green | [InChI]
InChI=1S/C13H15NO/c15-9-10-7-11-3-1-5-14-6-2-4-12(8-10)13(11)14/h7-9H,1-6H2 | [InChIKey]
XIIVBURSIWWDEO-UHFFFAOYSA-N | [SMILES]
C12=CC(C=O)=CC3=C1N(CCC3)CCC2 | [EPA Substance Registry System]
1H,5H-Benzo[ij]quinolizine- 9-carboxaldehyde, 2,3,6,7-tetrahydro-(33985-71-6) |
| Hazard Information | Back Directory | [Synthesis]
Julolidine (0.5 g, 2.89 mmol), N,N-dimethylformamide (0.255 g, 3.49 mmol), and phosphorous trichloride (0.535 g, 3.49 mmol) were dissolved in dichloromethane (15 mL), and the mixture was stirred for 4 h at room temperature under argon protection. The color of the solution changed to green during the reaction and the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction was quenched with water and the crude product was subsequently extracted with 2 M sodium hydroxide solution and ether. The organic phase was washed twice with water, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography with 40%-50% ether/hexane as eluent to give 0.48 g (83.08% yield) of 1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline-9-carboxaldehyde as a light-yellow solid (up to 92% when 1.5 g of julonidine was used). The structure of the product was confirmed by 1H NMR (300 MHz, CDCl3): δ 9.597 (s, 1H), 7.29 (s, 1H), 3.308 (t, J = 57 Hz, 4H), 2.787 (t, J = 62 Hz, 4H), 2.002-1.92 (m, J = 63 Hz, 4H). | [References]
[1] Tetrahedron, 2007, vol. 63, # 1, p. 103 - 114
[2] Organic Preparations and Procedures International, 2001, vol. 33, # 6, p. 603 - 613
[3] Journal of Nanoscience and Nanotechnology, 2015, vol. 15, # 11, p. 8813 - 8819
[4] Chemistry - A European Journal, 2010, vol. 16, # 30, p. 9257 - 9263
[5] Chemical Communications, 2014, vol. 50, # 78, p. 11507 - 11510 |
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