Pyridine → (2S)-1-acetyl-4-hydroxypyrrolidine-2-carboxylic acid
Reaction equation
[NH:1]1[CH2:9][C@H:7]([OH:8])[CH2:6][C@H:2]1[C:3]([OH:5])=[O:4].N1C=CC=CC=1.[C:16](OC(=O)C)(=[O:18])[CH3:17]>O>[C:16]([N:1]1[CH2:9][CH:7]([OH:8])[CH2:6][C@H:2]1[C:3]([OH:5])=[O:4])(=[O:18])[CH3:17]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 100 g (0.76 mol) of L-hydroxyproline and 540 ml of water was cooled to 10° and 297 ml (3.7 mol) of pyridine was added. The temperature was lowered to 5° and 151.2 ml (1.6 mol) of acetic anhydride was slowly added. The reaction was stirred at 0°-5° for 45 min and 81 ml (0.97 mol) of pyridine was added followed by 42.7 ml (0.45 mol) of acetic anhydride. The reaction was stirred overnight in an ice bath allowing the bath to come to room temperature. The reaction was evaporated and the residue was dissolved in ethanol and evaporated to an oily residue. This step was repeated a number of times, and the residue was dissolved in acetone, seeded, and cooled. The white crystals were filtered and recrystallized from ethanol-ether and dried under vacuum at 40° to give 84.8 g of N-acetyl-4-hydroxy-L-proline; mp 124°-131°; [α]D23 -117° (cl, water).
Workup
- customwas lowered to 5°
- stirringThe reaction was stirred overnight in an ice bath
- customto come to room temperature
- customThe reaction was evaporated
- dissolutionthe residue was dissolved in ethanol
- customevaporated to an oily residue
- dissolutionthe residue was dissolved in acetone
- temperaturecooled
- filtrationThe white crystals were filtered
- customrecrystallized from ethanol-ether
- customdried under vacuum at 40°
Sources & evidence
- ORD record
- ord-27d5fd94273243509fe3fd1ec062410b
- Source dataset
- uspto-grants-1981_07
- Patent number
- US04278681
Reaction notes
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