Sulfuric Acid → (4S)-4-cyclohexyl-L-proline
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]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- additionafter the addition, it
- filtrationThe reaction mixture was filtered through a Celite pad
- washwashed with 10 ml of acetic acid
- additionIsopropyl alcohol (2 ml) was added to the filtrate
- stirringstirred well
- customa clear solution decanted
- concentrationconcentrated to a thick oil
- dissolutionThe oil was dissolved in 5 ml of water
- additionthe pH was brought to 6.0 by the addition of concentrated ammonium hydroxide
- filtrationThe resultant precipitate was filtered
- washwashed with 5 ml of water and excess ether, and vacuum
- customdried
Sources & evidence
- ORD record
- ord-d4d5ef1ae06f4cf0aded14a48a8e1d8f
- Source dataset
- uspto-grants-1986_05
- Patent number
- US04588819
Reaction notes
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