Methylamine → rac-(1R,2R)-2-(methylamino)cyclohexan-1-ol

HRID 614565Notes

Reaction equation

HRID 614565 reaction equation
[CH:1]12[O:7][CH:2]1[CH2:3][CH2:4][CH2:5][CH2:6]2.[CH3:8][NH2:9].[OH-].[Na+]>>[CH3:8][NH:9][C@@H:1]1[CH2:6][CH2:5][CH2:4][CH2:3][C@H:2]1[OH:7]

Participants

4

Procedure

Cyclohexene oxide (196.28 g., 2 mole) is added during 30 min. to 40% aqueous methylamine (466 ml., 6 moles) with stirring. The temperature is from 25° to 27° during this addition. During the following 45 min. the temperature rises to 55° and is kept at 50° to 58° by occasional cooling. It is stirred at room temperature for 18 hr., then heated on the steam bath for 2 hrs., cooled and saturated with solid sodium hydroxide (NaOH). The mixture is extracted well with ether, the extract dried over magnesium sulfate (MgSO4) and evaporated through a 9" Vigreux. Distillation at 13 mm gives 241.9 g. (97% yield) of the title compound b.p. 100°-101° nmr in CDCl3 (100 MHz) is in accord; Mass spectrum M+ 129.

Workup

  1. additionThe temperature is from 25° to 27° during this addition
  2. customDuring the following 45 min.
  3. customrises to 55°
  4. customis kept at 50° to 58° by occasional cooling
  5. stirringIt is stirred at room temperature for 18 hr
  6. temperature, then heated on the steam bath for 2 hrs
  7. extractionThe mixture is extracted well with ether
  8. dry with materialthe extract dried over magnesium sulfate (MgSO4)
  9. customevaporated through a 9" Vigreux
  10. distillationDistillation at 13 mm
  11. customgives 241.9 g

Sources & evidence

ORD record
ord-8641a55dc3c44bc39ea75b3276f2f039
Source dataset
uspto-grants-1979_03
Patent number
US04145435

Reaction notes

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