2-INDANCARBOXYLIC ACID
2-INDANCARBOXYLIC ACID Basic information
- Product Name:
- 2-INDANCARBOXYLIC ACID
- Synonyms:
-
- 2-INDANCARBOXYLIC ACID
- 2-INDANECARBOXYLIC ACID
- CBI-BB ZERO/005363
- INDAN-2-CARBOXYLIC ACID
- Indancarboxylicacid
- 2-INDANCARBOXYLIC ACID 98+%
- TIMTEC-BB SBB003945
- 2-Carboxyindane
- CAS:
- 25177-85-9
- MF:
- C10H10O2
- MW:
- 162.19
- Product Categories:
-
- C10
- Carbonyl Compounds
- Carboxylic Acids
- Mol File:
- 25177-85-9.mol
2-INDANCARBOXYLIC ACID Chemical Properties
- Melting point:
- 128-132 °C (lit.)
- Boiling point:
- 192 °C / 18mmHg
- Density
- 1.0281 (rough estimate)
- refractive index
- 1.6000 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- pka
- 4.65±0.20(Predicted)
- form
- Crystalline Powder
- color
- White to cream or brown
- CAS DataBase Reference
- 25177-85-9(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
2-INDANCARBOXYLIC ACID Usage And Synthesis
Chemical Properties
White powder
Synthesis
26453-01-0
25177-85-9
General procedure for the synthesis of 2-indenecarboxylic acid from 2,3-dihydro-1H-indene-2-carbonitrile: A mixture of 2,3-dihydro-1H-indene-2-carbonitrile (128) (55.1 g, 0.385 mol), concentrated hydrochloric acid (100 mL), and dioxane (500 mL) was stirred for 41 hours at 60-70°C. Upon completion of the reaction, the mixture was cooled and the dioxane was removed by evaporation to give a residue. The residue was suspended in 1 M hydrochloric acid (300 mL) and stirred at 20 °C for 15 hours. Subsequently, the solid product was collected by filtration, washed with water and dried to give 2-indenecarboxylic acid (129) (54.1 g, 87% yield) as a white solid. Melting point (EtOAc/petroleum ether recrystallization) 128 °C [literature value (Baeyer, A. Perkin W.H., Chem. Ber. 1884, 17, 122) mp 130.2 °C]; 1H NMR (δ): 10.50 (broad single peak, 1H, COOH), 7.14-7.25 (multiple peaks, 4H, H-4, H-5, H -6, H-7), 3.21-3.43 (multiple peaks, 5H, H-1, H-2, H-3).
References
[1] Patent: WO2006/104406, 2006, A1. Location in patent: Page/Page column 112
[2] Journal of Medicinal Chemistry, 2008, vol. 51, # 21, p. 6853 - 6865
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