Isopropanol → trans-2-(2-Chlorophenylamino)cyclohexanol

HRID 1243047Notes

Reaction equation

HRID 1243047 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

7

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

  1. customcap
  2. customThe septum cap
  3. customlined cap
  4. customThe reaction mixture was transferred to a separatory funnel
  5. extractionextracted with methylene chloride (3×10 mL)
  6. washThe organics were washed with brine
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated
  9. customThe crude material was purified by silica gel chromatography
  10. 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

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