ChemicalBook--->CAS DataBase List--->2201-23-2

2201-23-2

2201-23-2 Structure

2201-23-2 Structure
IdentificationBack Directory
[Name]

1-Phenyl-1-cyclohexanecarbonitrile
[CAS]

2201-23-2
[Synonyms]

AKOS BBS-00005316
1-phenylcyclohexanecarbonitrile
1-PHENYL-1-CYCLOHEXANECARBONITRILE
1-Phenylcyclohexane-1-carbonitrile
Cyclohexanecarbonitrile, 1-phenyl-
1-Phenyl-1-cyclohexanecarbonitrile,97%
1-PHENYL-1-CYCLOHEXANECARBONITRILE 97%
[EINECS(EC#)]

218-608-1
[Molecular Formula]

C13H15N
[MDL Number]

MFCD00021281
[MOL File]

2201-23-2.mol
[Molecular Weight]

185.26
Chemical PropertiesBack Directory
[Appearance]

CLEAR COLOURLESS TO PALE BROWN LIQUID
[Boiling point ]

141°C/7mmHg(lit.)
[density ]

1.01
[refractive index ]

1.5332-1.5352
[Fp ]

121°
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[color ]

Colorless to Light yellow to Light orange
[InChI]

InChI=1S/C13H15N/c14-11-13(9-5-2-6-10-13)12-7-3-1-4-8-12/h1,3-4,7-8H,2,5-6,9-10H2
[InChIKey]

AUXIEQKHXAYAHG-UHFFFAOYSA-N
[SMILES]

C1(C2=CC=CC=C2)(C#N)CCCCC1
[NIST Chemistry Reference]

1-Phenyl-1-cyclohexanecarbonitrile(2201-23-2)
Hazard InformationBack Directory
[Chemical Properties]

CLEAR COLOURLESS TO PALE BROWN LIQUID
[Synthesis]

1,5-Dibromopentane

111-24-0

Benzeneacetonitrile

140-29-4

1-Phenyl-1-cyclohexanecarbonitrile

2201-23-2

GENERAL STEPS: A mixture of benzeneacetonitrile (50.0 g, 426.8 mmol) and 1,5-dibromopentane (58.1 mL, 426.8 mmol) was added slowly and dropwise to a dimethylsulfoxide (600.0 mL) suspension of NaH (42.7 g, 1067.0 mmol, 60%) at 0 °C. The mixture was pre-dissolved in a solvent mixture of dimethyl sulfoxide and ether (1:1, 200.0 mL). After dropwise addition, the reaction mixture was continued to be stirred at 0°C for 2 hours. Upon completion of the reaction, water and 10% HCl solution were added to the mixture, followed by extraction with ethyl acetate. The organic layers were combined, washed sequentially with water and brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to give the crude product. The crude product was purified by conventional silica gel column chromatography (eluent: hexane) to afford 1-phenyl-1-cyclohexanecarbonitrile (52.0 g, yield 65.76%) as a colorless oil.GC-MS analysis showed that the molecular ion peak m/z was 185.0.

[References]

[1] Patent: US2014/194431, 2014, A1. Location in patent: Paragraph 0940-0942
[2] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 14, p. 3913 - 3924
[3] Journal of Organic Chemistry, 1971, vol. 36, p. 1308 - 1309
[4] Chemische Berichte, 1973, vol. 106, p. 2890 - 2903
[5] Bulletin de la Societe Chimique de France, 1965, p. 2030 - 2037
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

36/37/38-20/21/22
[Safety Statements ]

36/37/39-26
[RIDADR ]

UN 3276 6.1/PG III
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29269095
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

1-Phenyl-1-cyclohexanecarbonitrile(2201-23-2).msds
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