Methyl iodide → HCID 2794227, compound
Reaction equation
[H-].[Na+].C(OC([NH:10][C@@H:11]([CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH2:12][OH:13])=O)(C)(C)C.CI.[Cl-].[NH4+].F[C:26](F)(F)C(O)=O>C1COCC1.C(Cl)Cl>[CH2:14]([C@H:11]([NH2:10])[CH2:12][O:13][CH3:26])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 2
Procedure
Sodium hydride (60% dispersion in oil: 322 mg, 8.1 mmol) was added to a stirred solution of N-tert-butoxycarbonyl-(S)-1-benzyl-1-aminoethan-2-ol (2.02 g, 8.1 mmol) in dry THF (50 ml) at 0° C. under argon. The mixture was stirred for 10 min. and methyl iodide (3 ml) added. The reaction mixture was allowed to warm to room temperature and stirred for 1 h. Saturated ammonium chloride (80 ml) was added and the mixture extracted with ethyl acetate (2×100 ml). The combined organic extracts were dried over anhydrous sodium sulphate, filtered and concentrated to give a clear oil. The oil was dissolved in DCM (40 ml) and treated with excess trifluoroacetic acid.(6.2 ml) at 0° C. The mixture was allowed to warm up to room temperature and was stirred for 2 h. The mixture was washed with aqueous sodium hydrogen carbonate and brine, and dried over anhydrous sodium sulphate. Filtration and evaporation gave (S)-1-benzyl-2-methoxyethylamine (620 mg, 47%) as a colourless oil.
Workup
- stirringstirred for 1 h
- extractionthe mixture extracted with ethyl acetate (2×100 ml)
- dry with materialThe combined organic extracts were dried over anhydrous sodium sulphate
- filtrationfiltered
- concentrationconcentrated
- customto give a clear oil
- customat 0° C
- temperatureto warm up to room temperature
- stirringwas stirred for 2 h
- washThe mixture was washed with aqueous sodium hydrogen carbonate and brine
- dry with materialdried over anhydrous sodium sulphate
- filtrationFiltration and evaporation
Sources & evidence
- ORD record
- ord-931e771a9a404925ba4ed2e4db2720cd
- Source dataset
- uspto-grants-1994_01
- Patent number
- US05276153
Reaction notes
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