(1R)-2-Chloro-1-(pyridin-3-yl)ethan-1-ol → (R)-2-chloro-1-pyridin-3-ylethan-1-ol hydrochloride
Reaction equation
[Cl:1][CH2:2][C@@H:3]([C:5]1[CH:6]=[N:7][CH:8]=[CH:9][CH:10]=1)[OH:4]>Cl.C(OC)(C)(C)C>[ClH:1].[Cl:1][CH2:2][C@@H:3]([C:5]1[CH:6]=[N:7][CH:8]=[CH:9][CH:10]=1)[OH:4]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The thus-obtained (R)-2-chloro-1-pyridin-3-ylethan-1-ol was dissolved in a methanolic hydrochloric acid solution, methyl tert-butyl ether was then gradually added drop wise, and the mixture was stirred at room temperature for 1 hour. The resulting white precipitate was filtered off to give 1.04 g of (R)-2-chloro-1-pyridin-3-ylethan-1-ol hydrochloride as white crystals. The optical purity was 99.7% ee.
Workup
- filtrationThe resulting white precipitate was filtered off
Sources & evidence
- ORD record
- ord-7110ac34c3da45f196721139d9f9f74f
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06515134B1
Reaction notes
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