9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine
9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine Basic information
- Product Name:
- 9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine
- Synonyms:
-
- 8-Hydroxy-1,1,7,7-tetramethyl-1,2,3,5,6,7-hexahydro-pyrido[3,2,1-ij]quinoline-9-carbaldehyde
- 9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine
- 8-HYDROXY-1,1,7,7-TETRAMETHYL-2,3,6,7-TETRAHYDRO-1H,5H-PYRIDO[3,2,1-IJ]QUINOLINE-9-CARBOXALDEHYDE
- 8-HYDROXY-1,1,7,7-TETRAMETHYLJULOLIDINE-9-CARBOXALDEHYDE
- 8-HYDROXY-1,1,7,7-TETRAMETHYLJULOLIDINE-9-CARBOXALDEHYDE 99%
- 8-Hydroxy-1,1,7,7-tetramethyljulolidine-9-carboxaldehyde,99%
- 1,1,7,7-Tetramethyl-8-hydroxy-9-formyljulolidine
- 9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine 2,3,6,7-Tetrahydro-8-hydroxy-1,1,7,7-tetramethyl-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde
- CAS:
- 115662-09-4
- MF:
- C17H23NO2
- MW:
- 273.37
- Product Categories:
-
- Quinoline&Isoquinoline
- Mol File:
- 115662-09-4.mol
9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine Chemical Properties
- Melting point:
- 74-77 °C
- Boiling point:
- 416.39°C (rough estimate)
- Density
- 1.0101 (rough estimate)
- refractive index
- 1.5200 (estimate)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 9.50±0.60(Predicted)
- color
- White to Light yellow to Green
Safety Information
- Safety Statements
- 24/25
- HS Code
- 29339900
MSDS
- Language:English Provider:ACROS
9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine Usage And Synthesis
Chemical Properties
Light Green Crystals
Synthesis
115704-83-1
68-12-2
115662-09-4
GENERAL METHODS: 8-Hydroxy-1,1,7,7-tetramethyl-2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinoline-8-ol and N,N-dimethylformamide were used as raw materials to synthesize 8-hydroxy-1,1,7,7-tetramethyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline-9-carbaldehyde. The procedure was as follows: to a magnetically stirred solution of N,N-dimethylformamide (2 mL, 23 mmol) of phosphorous trichloride (2.2 mL, 23 mmol) under argon protection, 1,1,7,7-tetramethyl-2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-8-aldehyde (2 g, 11.6 mmol) was slowly added at 0°C and additional of N,N-dimethylformamide (2 mL). Subsequently, the reaction mixture was stirred at room temperature for 3 h and the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was neutralized with ammonium hydroxide solution and then the product was extracted with ethyl acetate. The organic phase was washed several times with water to remove impurities. Finally, the residue was purified by column chromatography (silica gel as stationary phase and 10% ethyl acetate/hexane as eluent) to afford the target product 8-hydroxy-1,1,7,7-tetramethyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline-9-carboxaldehyde in a yield of 1.8 g (80% yield).
References
[1] Molecular Crystals and Liquid Crystals, 2008, vol. 491, p. 152 - 163
[2] Tetrahedron Letters, 2018, vol. 59, # 29, p. 2788 - 2792
9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine Preparation Products And Raw materials
Raw materials
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9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine(115662-09-4)Related Product Information
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- 3-(trifluoromethyl) Cinnamaldehyde
- CHLOROPHOSPHONAZO III
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- 8-HYDROXYJULOLIDINE
- 2,6-DIISOPROPYL-N,N-DIMETHYLANILINE
- 4-Diethylaminobenzaldehyde
- 3-Ethylamino-4-methylphenol
- 1-METHYL-1,2,3,4-TETRAHYDRO-QUINOLINE-6-CARBALDEHYDE
- 2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde
- 3-TERT-BUTYL-2-HYDROXYBENZALDEHYDE
- 3,5-Di-tert-butylsalicylaldehyde
- N,N,2,4,6-PENTAMETHYLANILINE
- 4,6-DI-TERT-BUTYL-2-METHYLPHENOL
- 6-METHYL-1,2,3,4-TETRAHYDROQUINOLINE
- 1,1,7,7-Tetramethyljulolidine-9-carboxaldehyde
- 7-Hydroxy-1,2,3,4-tetrahydroquinoline