| Identification | Back Directory | [Name]
1-cyclopropylnaphthalene | [CAS]
25033-19-6 | [Synonyms]
1-Naphthylcyclopropane
1-cyclopropylnapthalene
1-cyclopropylnaphthalene
Naphthalene, 1-cyclopropyl- | [EINECS(EC#)]
690-694-7 | [Molecular Formula]
C13H12 | [MDL Number]
MFCD00760297 | [MOL File]
25033-19-6.mol | [Molecular Weight]
168.23 |
| Hazard Information | Back Directory | [Uses]
1-Cyclopropylnaphthalene can be a starting material in the synthesis of 3-hydroxy-3-naphthyl-propyl nitrate. 1-Cyclopropylnaphthalene is a derivative of Naphthalene (N345600). Naphthalene is an abundant polycyclic aromatic hydrocarbon that is persistent, bioaccumulative, toxic and found in tobacco smoke and urban air. | [Synthesis]
General procedure for the synthesis of 1-cyclopropylnaphthalene from 1-bromonaphthalene and cyclopropylmagnesium bromide: Cyclopropylmagnesium bromide (150 mL, 0.5 M in tetrahydrofuran) was added slowly and dropwise to a solution of tetrahydrofuran (10 mL) containing 1-bromonaphthalene (10 g, 50 mmol) and [1,3-bis(diphenylphosphino)propane]nickel(II) dichloride at 0 °C. The reaction mixture was stirred at room temperature for 16 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was extracted by adding ethyl acetate and aqueous ammonium chloride solution to the residue. The organic layer was separated, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Finally, the residue was purified by silica gel column chromatography to afford 1-cyclopropylnaphthalene (6.4 g, 76% yield). | [References]
[1] Patent: WO2009/70740, 2009, A2. Location in patent: Page/Page column 89
[2] Patent: WO2006/26356, 2006, A2. Location in patent: Page/Page column 20
[3] Patent: WO2011/85009, 2011, A2. Location in patent: Page/Page column 36
[4] Patent: WO2014/8295, 2014, A1. Location in patent: Paragraph 0345-0348 |
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