2-Methylindene
2-Methylindene Basic information
- Product Name:
- 2-Methylindene
- Synonyms:
-
- 2-METHYL-1H-INDENE
- 2-METHYL-1H-INDENE 98+%
- 2-METHYLINDENE
- 2-Methylindene 98%
- 1H-Indene, 2-methyl-
- Indene, 2-methyl-
- indene,2-methyl-
- CAS:
- 2177-47-1
- MF:
- C10H10
- MW:
- 130.19
- Product Categories:
-
- Arenes
- Building Blocks
- Organic Building Blocks
- Indanone & Indene
- Mol File:
- 2177-47-1.mol
2-Methylindene Chemical Properties
- Melting point:
- 80°C
- Boiling point:
- 45 °C0.2 mm Hg(lit.)
- Density
- 0.971 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.567(lit.)
- Flash point:
- 169 °F
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- Colorless to light yellow Liquid
- InChI
- InChI=1S/C10H10/c1-8-6-9-4-2-3-5-10(9)7-8/h2-6H,7H2,1H3
- InChIKey
- YSAXEHWHSLANOM-UHFFFAOYSA-N
- SMILES
- C1C2=C(C=CC=C2)C=C1C
- CAS DataBase Reference
- 2177-47-1(CAS DataBase Reference)
- NIST Chemistry Reference
- 2-Methylindene(2177-47-1)
MSDS
- Language:English Provider:2-Methylindene
- Language:English Provider:SigmaAldrich
2-Methylindene Usage And Synthesis
Chemical Properties
transparent to yellow liquid
Synthesis
17496-14-9
2177-47-1
The general procedure for the synthesis of 2-methylindene (6) from 2-methylindan-1-one (5) was as follows: 5.0 g (34 mmol) of 2-methyl-1-indanone (5) was reacted with 1.94 g (51 mmol) of NaBH4 in a reduction reaction according to the method of Example G. Subsequently, the unpurified alcohol was further reacted in 100 g of toluene catalyzed by 0.2 g of p-toluenesulfonic acid at 80 °C. The reaction mixture was purified by column chromatography on 100 g silica gel with hexane/dichloromethane (9:1) as eluent to give 3.68 g (82% yield) of the target product 2-methylindene (6). The product was characterized by 1H-NMR (100 MHz, CDCl3): δ 7.2 (4H, m), 6.45 (1H, m), 3.25 (2H, m), 2.1 (3H, m). Mass spectrometry analysis showed a molecular ion peak of 130 M+ and a cleavage pattern as expected.
References
[1] Journal of Chemical Research, 2010, # 6, p. 325 - 329
[2] Journal of Organic Chemistry, 1980, vol. 45, # 23, p. 4564 - 4572
[3] Journal of Organic Chemistry, 1984, vol. 49, # 22, p. 4226 - 4237
[4] Journal of Organic Chemistry, 1982, vol. 47, # 6, p. 1051 - 1058
[5] Collection of Czechoslovak Chemical Communications, 1983, vol. 48, # 1, p. 60 - 70
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