Hydrochloric Acid → Methyl (2S,4R)-4-hydroxy-1-methyl-2-pyrrolidinecarboxylate hydrochloride
Reaction equation
[ClH:1].[OH:2][C@H:3]1[CH2:7][N:6]([CH3:8])[C@H:5]([C:9]([OH:11])=[O:10])[CH2:4]1.[CH3:12]O>>[ClH:1].[OH:2][C@H:3]1[CH2:7][N:6]([CH3:8])[C@H:5]([C:9]([O:11][CH3:12])=[O:10])[CH2:4]1Participants
4
Procedure
Concentrated hydrochloric acid (3 mL) was added to a suspension of (2S,4R)-4-hydroxy-1-methyl-2-pyrrolidinecarboxylic acid (3 g) in methanol (15 mL), and the mixture was refluxed for 4 hours. The solvent of the reaction mixture was removed by distillation under reduced pressure to give the title compound (4.0 g, yield 100%).
Workup
- temperaturethe mixture was refluxed for 4 hours
- customThe solvent of the reaction mixture was removed by distillation under reduced pressure
Sources & evidence
- ORD record
- ord-3d46b2f5ddc04d9f8ad15119131b08ac
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07034150B2
Reaction notes
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