ChemicalBook--->CAS DataBase List--->5851-46-7

5851-46-7

5851-46-7 Structure

5851-46-7 Structure
IdentificationBack Directory
[Name]

1H-Benzimidazole,2-pentyl-(9CI)
[CAS]

5851-46-7
[Synonyms]

2-Pentylbenzimidazole
2-amyl-1H-benzimidazole
2-Pentyl-1H-benzoimidazole
1H-BenziMidazole, 2-pentyl-
2-pentyl-1H-benzimidazole v
2-Pentyl-1H-benzo[d]imidazole
1H-Benzimidazole,2-pentyl-(9CI)
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C12H16N2
[MOL File]

5851-46-7.mol
[Molecular Weight]

188.27
Chemical PropertiesBack Directory
[Melting point ]

155-156 °C
[Boiling point ]

250 °C
[density ]

1.061±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

11.99±0.10(Predicted)
[InChI]

InChI=1S/C12H16N2/c1-2-3-4-9-12-13-10-7-5-6-8-11(10)14-12/h5-8H,2-4,9H2,1H3,(H,13,14)
[InChIKey]

OYGJENONTDCXGW-UHFFFAOYSA-N
[SMILES]

C1(CCCCC)NC2=CC=CC=C2N=1
Spectrum DetailBack Directory
[Spectrum Detail]

1H-Benzimidazole,2-pentyl-(9CI)(5851-46-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Hexanal

66-25-1

o-Phenylenediamine

95-54-5

1H-Benzimidazole,2-pentyl-(9CI)

5851-46-7

Under an open oxygen atmosphere, 1,2-phenylenediamine (1.0 mmol) was dissolved with hexanal (1.2 mmol) in ethanol (3 mL), followed by the addition of 10 mol% of catalyst. The reaction mixture was stirred at room temperature until the reaction was complete (see Table 2 for reaction times). The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was diluted with ethanol (20 mL) and the catalyst was removed by filtration. Subsequently, the organic layer was concentrated under reduced pressure and the crude product obtained was purified by silica gel column chromatography with the eluent being a solvent mixture of ethyl acetate and n-hexane (1:9, v/v), resulting in pure 2-pentyl-1H-benzo[d]imidazole. The spectral data of the product were in agreement with those reported in the literature [48], [54] and [55].

[References]

[1] Synthetic Communications, 2011, vol. 41, # 1, p. 58 - 62
[2] Tetrahedron Letters, 2011, vol. 52, # 43, p. 5575 - 5580
[3] Tetrahedron Letters, 2015, vol. 56, # 48, p. 6795 - 6799
[4] Tetrahedron Letters, 2007, vol. 48, # 1, p. 61 - 64
[5] Journal of Heterocyclic Chemistry, 2010, vol. 47, # 1, p. 153 - 155
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