2-Chloropyridine → 2-(N-Methyl-N-(2-pyridyl)amino)ethanol
Reaction equation
Cl[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[CH3:8][NH:9][CH2:10][CH2:11][OH:12]>O>[CH3:8][N:9]([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1)[CH2:10][CH2:11][OH:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-chloropyridine (12 g) and 2-(methylamino)ethanol (100 ml) are stirred under nitrogen at 120° C. for 18 hours. Cool to room temperature and then pour into iced water (250 ml). Extract with ethyl acetate (2×200 ml). Dry over sodium sulfate. Filter. Evaporate to dryness. The crude product is distilled in vacuo to give 10.3 g of N-methyl-N-(2-pyridinyl)-2-aminoethanol, boiling at 110° C./1.0 mmHg.
Workup
- extractionExtract with ethyl acetate (2×200 ml)
- dry with materialDry over sodium sulfate
- filtrationFilter
- customEvaporate to dryness
- distillationThe crude product is distilled in vacuo
Sources & evidence
- ORD record
- ord-c0c44e9beaef435bba9db6191c53fb0f
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06680387B2
Reaction notes
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