Cyclohexene oxide → rel-(1R,2R)-2-(1-Pyrrolidinyl)cyclohexanol

HRID 1846413Notes

Reaction equation

HRID 1846413 reaction equation
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:6]12[O:12][CH:7]1[CH2:8][CH2:9][CH2:10][CH2:11]2>O>[N:1]1([C@@H:6]2[CH2:11][CH2:10][CH2:9][CH2:8][C@H:7]2[OH:12])[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

4

Reactant 2

HCID 9246Cyclohexene oxideHCID 31268Pyrrolidine

Product 1

HCID 10103566rel-(1R,2R)-2-(1-Pyrrolidinyl)cyclohexanolYield 98%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
90 °C

Procedure

Pyrrolidine (4.26 g, 60 mmol) was added to a solution of cyclohexene oxide (1.96 g, 20 mmol) in H2O (6 mL), and the resulting mixture was heated at 90° C. for 16 hours. After cooling, the solvent was removed under reduced pressure and the resulting residue was extracted with DCM (10 mL×3). The organic phases were combined and dried with anhydrous Na2SO4. After removing the Na2SO4 by filtration, the solvent was evaporated and the material dried under vacuum to afford the desired compound (+/−)-1 (3.3 g, 19.5 mmol, yield 98%). 1H NMR (CDCl3) δ 4.06 (s, 1H), 3.45-3.30 (m, 1H), 2.75-2.63 (m, 2H), 2.62-2.50 (m, 2H), 2.51-2.42 (m, 1H), 1.90-1.58 (m, 8H), 1.45-1.15 (m, 4H).

Workup

  1. temperatureAfter cooling
  2. customthe solvent was removed under reduced pressure
  3. extractionthe resulting residue was extracted with DCM (10 mL×3)
  4. dry with materialdried with anhydrous Na2SO4
  5. customAfter removing the Na2SO4
  6. filtrationby filtration
  7. customthe solvent was evaporated
  8. customthe material dried under vacuum

Sources & evidence

ORD record
ord-b50f77da268245bcb28d70fd7e4ac310
Source dataset
uspto-grants-2015_02
Patent number
US08952032B2

Reaction notes

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