1,2,3,4-TETRAHYDRO-6-QUINOLINECARBOXYLIC ACID
1,2,3,4-TETRAHYDRO-6-QUINOLINECARBOXYLIC ACID Basic information
- Product Name:
- 1,2,3,4-TETRAHYDRO-6-QUINOLINECARBOXYLIC ACID
- Synonyms:
-
- 1,2,3,4-TETRAHYDRO-6-QUINOLINECARBOXYLIC ACID
- Tetrahydroquinoline-6-carboxylic acid
- 6-Carboxy-1,2,3,4-tetrahydroquinoline
- 1,2,3,4-Tetrahydroquinoline-6-carboxylic acid
- 1,2,3,4-Tetrahydroquinoline-6-carboxylic acid 95+%
- 6-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-
- 1,2,3,4-Tetrahydro-6-quinolinecarboxylic
- 1,2,3,4-Tetrahydro-6-quinolinecarboxylicAci
- CAS:
- 5382-49-0
- MF:
- C10H11NO2
- MW:
- 177.2
- Mol File:
- 5382-49-0.mol
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1,2,3,4-TETRAHYDRO-6-QUINOLINECARBOXYLIC ACID Chemical Properties
- Melting point:
- 168 °C
- Boiling point:
- 382.6±31.0 °C(Predicted)
- Density
- 1.223±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 4.96±0.20(Predicted)
- Appearance
- Off-white to yellow Solid
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1,2,3,4-TETRAHYDRO-6-QUINOLINECARBOXYLIC ACID Usage And Synthesis
Synthesis Reference(s)
The Journal of Organic Chemistry, 39, p. 2044, 1974 DOI: 10.1021/jo00928a014
Synthesis
851202-94-3
5382-49-0
GENERAL STEPS: 1-Acetyl-1,2,3,4-tetrahydroquinoline-6-carbonitrile (50 mmol) was dissolved in 8 M hydrochloric acid (150 mL) and the reaction was carried out at reflux for 18 hours. Upon completion of the reaction, the mixture was cooled and the pH was adjusted with sodium hydroxide solution to about 3. The precipitated 1,2,3,4-tetrahydroquinoline-6-carboxylic acid was separated by filtration, washed with water and dried. Yield: 61%.1H NMR (D6-DMSO) δ: 1.79 (m, 2H), 2.68 (m, 2H), 3.23 (m, 2H), 5.45 (br, 1H), 6.48 (d, 1H), 7.45-7.50 (m, 2H).
References
[1] Patent: WO2005/39572, 2005, A1. Location in patent: Page/Page column 31-32
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