Hydrochloric Acid → 928322-40-1
Reaction equation
[OH:1][CH:2]1[CH2:7][CH2:6][N:5]([CH:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:9]([O:11]CC)=[O:10])[CH2:4][CH2:3]1.[ClH:20]>>[ClH:20].[OH:1][CH:2]1[CH2:3][CH2:4][N:5]([CH:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:9]([OH:11])=[O:10])[CH2:6][CH2:7]1Participants
3
Procedure
A suspension of ethyl (4-hydroxypiperidin-1-yl)(phenyl)acetate (5.2 g) in 6N hydrochloric acid (80 mL) was refluxed for 14 hours and the mixture was evaporated in vacuo. The residue was triturated with methanol and collected by filtration and dried in vacuo to afford (4-hydroxypiperidin-1-yl) (phenyl)acetic acid hydrochloride (4.65 g) as a powder.
Workup
- temperaturewas refluxed for 14 hours
- customthe mixture was evaporated in vacuo
- customThe residue was triturated with methanol
- filtrationcollected by filtration
- customdried in vacuo
Sources & evidence
- ORD record
- ord-3b136036407546e98f5087189c191397
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08211919B2
Reaction notes
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