Ethanolamine → HCID 33787778, compound

HRID 2403976Notes

Reaction equation

HRID 2403976 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

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

  1. concentrationThe reaction mixture was concentrated
  2. additionthe resulting residue was diluted with DCM (70 mL)
  3. customThe organic layer was partitioned with water (70 mL)
  4. extractionthe aqueous layer extracted with DCM
  5. dry with materialCombined organic layers, dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-139810e0e2804c1badc26854d88d576e
Source dataset
uspto-grants-2014_08
Patent number
US08802698B2

Reaction notes

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