Ethanolamine → 1-(2-Hydroxyethyl)-2,5-dimethylpyrrole

HRID 1611414Notes

Reaction equation

HRID 1611414 reaction equation
[CH3:1][C:2](=O)[CH2:3][CH2:4][C:5](=O)[CH3:6].[CH2:9]([CH2:11][NH2:12])[OH:10].C(O)(=O)C(C)(C)C.CCCCCCC.O1CCCC1.C1(C)C=CC=CC=1>ClCCl.O>[OH:10][CH2:9][CH2:11][N:12]1[C:2]([CH3:1])=[CH:3][CH:4]=[C:5]1[CH3:6]

Participants

7

Conditions

Temperature
115 °C

Procedure

A mixture of hexan-2,5-dione (5 g), ethanol amine (26.7 g) and pivalic acid (23.26 g) in a solvent mixture containing n-heptane: tetrahydrofuran: toluene (4:1:1, 50 mL) was refluxed with stirring at 110-120° C. Water formed during the reaction was removed azeotropically during 3 to 4 hrs. The reaction mixture was cooled and the solvent was removed. The residue obtained was dissolved in dichloromethane (30 mL), washed with saturated sodium bicarbonate solution (30 mL), water (30 mL), and then with brine (30 mL), dried (Na2SO4) and the solvent was evaporated. The crude compound obtained as an oily mass, was purified by column chromatography (silica gel 100-200), using ethyl acetate:hexane (2:8) as an eluent to obtain the title compound.

Workup

  1. temperaturewas refluxed
  2. customwas removed azeotropically during 3 to 4 hrs
  3. temperatureThe reaction mixture was cooled
  4. customthe solvent was removed
  5. customThe residue obtained
  6. washwashed with saturated sodium bicarbonate solution (30 mL), water (30 mL)
  7. dry with materialwith brine (30 mL), dried (Na2SO4)
  8. customthe solvent was evaporated
  9. customThe crude compound obtained as an oily mass
  10. customwas purified by column chromatography (silica gel 100-200)

Sources & evidence

ORD record
ord-a25a12d337ab49a49afe1cbda1892f18
Source dataset
uspto-grants-2006_01
Patent number
US06987123B2

Reaction notes

Loading…