Ethanolamine → HCID 33787778, compound
Reaction equation
Br[CH2:2][CH:3]([CH2:6][CH3:7])[CH2:4][CH3:5].[CH2:8]([CH2:10][NH2:11])[OH:9]>C(O)C>[CH2:4]([CH:3]([CH2:6][CH3:7])[CH2:2][NH:11][CH2:10][CH2:8][OH:9])[CH3:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 75 °C
Procedure
A mixture of 3-bromomethyl-pentane (6.0 g, 36.4 mmol) and ethanolamine (13 mL, 218 mmol) in ethanol (45 mL) was heated at 75° C. for 16 h. The reaction mixture was concentrated and the resulting residue was diluted with DCM (70 mL). The organic layer was partitioned with water (70 mL) and the aqueous layer extracted with DCM. Combined organic layers, dried over magnesium sulfate, filtered, and concentrated to give the title compound as an oil (4.90 g). 1H NMR (d6-DMSO, 400 MHz) δ (ppm): 3.44 (t, J=5.6 Hz, 2H), 2.54 (t, J=6.0 Hz, 2H), 2.40 (d, J=5.6 Hz, 2H), 1.31-1.25 (m, 5H), 0.83 (t, J=6.8 Hz, 6H).
Workup
- concentrationThe reaction mixture was concentrated
- additionthe resulting residue was diluted with DCM (70 mL)
- customThe organic layer was partitioned with water (70 mL)
- extractionthe aqueous layer extracted with DCM
- dry with materialCombined organic layers, dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-139810e0e2804c1badc26854d88d576e
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08802698B2
Reaction notes
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