Ethylene Oxide → 2-[(2-hydroxyethyl)amino]-2-methylpropan-1-ol
Reaction equation
[NH2:1][C:2]([CH3:6])([CH3:5])[CH2:3][OH:4].[CH2:7]1[O:9][CH2:8]1>O>[OH:9][CH2:8][CH2:7][NH:1][C:2]([CH3:6])([CH3:5])[CH2:3][OH:4]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(2-Hydroxy-ethylamino)-2-methyl-propan-1-ol was prepared from 2-amino-2-methyl-propan-1-ol following a modified procedure from Cottle et al. J. Chem. Soc. 1946, 289. To a solution of 2-amino-2-methyl-propan-1-ol (250 mL, 2.61 mol, 1.76 equiv.) in H2O (400 mL) at −5° C. (external temperature, NaCl/ice bath) was added ethylene oxide (65.25 g, 1.48 mol, condensed at −78° C.). The solution was stirred over 16 hours, during which time the temperature warmed to room temperature. The H2O was removed in vacuo and the remaining 2-amino-2-methyl-propan-1-ol was distilled. The crude residue was dissolved in boiling EtOAc and precipitated with the addition of hexanes to provide 2-(2-Hydroxy-ethylamino)-2-methyl-propan-1-ol (145.5 g, 74%) as colorless crystals. LC/MS found 134.03 (M++H, C6H16NO2 requires 134.12).
Workup
- customThe H2O was removed in vacuo
- distillationthe remaining 2-amino-2-methyl-propan-1-ol was distilled
- dissolutionThe crude residue was dissolved
- customprecipitated with the addition of hexanes
Sources & evidence
- ORD record
- ord-02be4e1030ca4feda70fa3bd4ddac051
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08809266B2
Reaction notes
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