Isopropanol → trans-2-(2-Chlorophenylamino)cyclohexanol
Reaction equation
[OH-].[Na+].Cl.[NH2:4][CH:5]1[CH2:10][CH2:9][CH2:8][CH2:7][CH:6]1[OH:11].[Cl:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1I.C(O)(C)C>[Cl-].[Na+].O.[Cu]I>[Cl:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[NH:4][C@@H:5]1[CH2:10][CH2:9][CH2:8][CH2:7][C@H:6]1[OH:11]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 90 °C
Procedure
A 15 mL screw top test tube fitted with a PTFE septum cap was purged with argon before addition of CuI (5.0 mg, 0.026 mmol, 2.6 mol %), NaOH (125 mg, 3.12 mmol) and rac-2-amino-1-cyclohexanol HCl (158 mg, 1.04 mmol). 2-Chloro-1-iodobenzene (152 μL, 1.25 mmol) and isopropyl alcohol (1.0 mL) were added, via syringe, under argon. The septum cap was replaced with a solid, Teflon-lined cap and the reaction was stirred magnetically at 90° C. for 48 h. The resulting homogeneous solution was allowed to cool before dilution with 10 mL brine. The reaction mixture was transferred to a separatory funnel and extracted with methylene chloride (3×10 mL). The organics were washed with brine, dried over MgSO4 and concentrated. The crude material was purified by silica gel chromatography using hexanes/ethyl acetate (60:40). The product was obtained as a yellow oil in 91% yield (212.7 mg).
Workup
- customcap
- customThe septum cap
- customlined cap
- customThe reaction mixture was transferred to a separatory funnel
- extractionextracted with methylene chloride (3×10 mL)
- washThe organics were washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated
- customThe crude material was purified by silica gel chromatography
- customThe product was obtained as a yellow oil in 91% yield (212.7 mg)
Sources & evidence
- ORD record
- ord-5904c8bb0fb74a948fc75f0e7e0db299
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115784B2
Reaction notes
Loading…