Sulfuric Acid → (4S)-4-cyclohexyl-L-proline

HRID 280386Notes

Reaction equation

HRID 280386 reaction equation
CC(C)=[O:3].OS(O)(=O)=O.O=[Cr](=O)=O.S(=O)(=O)(O)O.[CH:19]1([C@H:25]2[CH2:29][NH:28][C@H:27]([CH2:30][OH:31])[CH2:26]2)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1>C(O)(=O)C>[CH:19]1([C@H:25]2[CH2:29][NH:28][C@H:27]([C:30]([OH:3])=[O:31])[CH2:26]2)[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]1

Participants

5

Procedure

To a solution of Jones reagent (2 ml) was added sulfuric acid (0.5 ml) and acetic acid (2.5 ml). (2S-trans)-4-Cyclohexyl-2-pyrrolidinemethanol (0.5 g) in 5 ml of acetic acid was added to the above solution and after the addition, it was stirred at room temperature for 15 minutes. The reaction mixture was filtered through a Celite pad and washed with 10 ml of acetic acid. Isopropyl alcohol (2 ml) was added to the filtrate, stirred well, and a clear solution decanted and concentrated to a thick oil. The oil was dissolved in 5 ml of water and the pH was brought to 6.0 by the addition of concentrated ammonium hydroxide. The resultant precipitate was filtered, washed with 5 ml of water and excess ether, and vacuum dried to yield 0.42 g of (trans)-4-cyclohexyl-L-proline as a pink solid, which was crystallized from methanol to obtain colorless crystals.

Workup

  1. additionafter the addition, it
  2. filtrationThe reaction mixture was filtered through a Celite pad
  3. washwashed with 10 ml of acetic acid
  4. additionIsopropyl alcohol (2 ml) was added to the filtrate
  5. stirringstirred well
  6. customa clear solution decanted
  7. concentrationconcentrated to a thick oil
  8. dissolutionThe oil was dissolved in 5 ml of water
  9. additionthe pH was brought to 6.0 by the addition of concentrated ammonium hydroxide
  10. filtrationThe resultant precipitate was filtered
  11. washwashed with 5 ml of water and excess ether, and vacuum
  12. customdried

Sources & evidence

ORD record
ord-d4d5ef1ae06f4cf0aded14a48a8e1d8f
Source dataset
uspto-grants-1986_05
Patent number
US04588819

Reaction notes

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