Nitric Acid → HCID 178500687, compound
Reaction equation
[N+:1]([O-:4])(O)=[O:2].S(=O)(=O)(O)O.[C:10]1([C@H:16]2[CH2:21][CH2:20][C@H:19]([CH2:22][C:23]([O:25][CH3:26])=[O:24])[CH2:18][CH2:17]2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>C(Cl)(Cl)(Cl)Cl>[N+:1]([C:13]1[CH:14]=[CH:15][C:10]([C@H:16]2[CH2:17][CH2:18][C@H:19]([CH2:22][C:23]([O:25][CH3:26])=[O:24])[CH2:20][CH2:21]2)=[CH:11][CH:12]=1)([O-:4])=[O:2]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 65% nitric acid (3.95 mL) and 95% sulphuric acid (4.97 mL) was added dropwise to a stirred solution of methyl (trans-4-phenylcyclohexyl)acetate (4710 mg) in CCl4 (20 mL) at 5° C. and the solution was allowed to warm to ambient temperature and stirred for 16 hours. Ice/water (50 mL) was added and the mixture was extracted with DCM (2×40 mL). The organic extracts were combined, washed with brine (50 mL), dried, and concentrated in vacuo to give an oil. This oil was purified by flash chromatography on a 80 g Biotage™ silica column, using a gradient of 0-20% EtOAc in hexane as the eluent to give crude methyl [trans-4-(4-nitrophenyl)cyclohexyl]acetate which was dissolved in ethyl acetate (30 mL). 10% palladium on carbon (0.400 g) was added and the resulting suspension was stirred at ambient temperature for 16 hours under an atmosphere of hydrogen. The suspension was filtered through diatomaceous earth and concentrated in vacuo to give a solid. This was purified by flash chromatography on a 40 g Biotage™ silica column using a gradient of 20-45% EtOAc/hexane as eluent to give the title compound (1740 mg) as a solid; 1H NMR δ 6.83 (2H, d), 6.46 (2H, d), 4.72 (2H, s), 3.59 (3H, s), 2.23 (3H, m), 1.72 (5H, m), 1.35 (2H, m), 1.09 (2H, m); MS m/e MH+ 248.
Workup
- extractionthe mixture was extracted with DCM (2×40 mL)
- washwashed with brine (50 mL)
- customdried
- concentrationconcentrated in vacuo
- customto give an oil
- customThis oil was purified by flash chromatography on a 80 g Biotage™ silica column
Sources & evidence
- ORD record
- ord-712757450d6f43eaa38796fef10fb0c2
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07795283B2
Reaction notes
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