Ethanolamine → Hydroxy ethylmaleimide
Reaction equation
[CH2:1]([CH2:3][NH2:4])O.C1[CH:10]2[O:11]C([CH:8]3[C:15](=O)[O:14]C(=O)[CH:9]32)C=1.C([OH:19])C>>[OH:14][CH2:15][CH2:8][C:9]1[C:10]([NH:4][C:3](=[O:19])[CH:1]=1)=[O:11]Participants
Conditions
- Temperature
- 0 °C
Procedure
Ethanolamine (80.96 g, 1.32 mol) was added to 500 mL of ethanol and cooled to 0° C. using an ice bath. 3,6-Endoxo-1,2,3,6-tetrahydrophthalic anhydride (220.21 g, 1.32 mol) was added to the solution and allowed to stir overnight. The yellow tinted crystals were used without purification. The solution was refluxed for four hours with azeotropic removal of water. The solution was cooled to 0° C. and the resulting crystals filtered (151.74 g, 54.95%). Removal of furan was facilitated by refluxing the crystals in xylenes for 4 hours with quantitative yield of hydroxy ethylmaleimide after purification by sublimation to yield white crystals, —CH2O—), 134.2 (2C, —CH═CH—), 171.2 (2C, —NC═O m.p. 68° C. 1H-NMR (CDCl3, δ, ppm): 2.62 (1H, —OH, s), 3.82-3.77 (4H, —NCH2CH2O—, overlapping), 6.76 (2H, —CH═CH—, s). 13C-NMR (CDCl3, δ, ppm): 40.5 (1C, —NCH2—), 60.5 (1C,).
Workup
- customThe yellow tinted crystals were used without purification
- temperatureThe solution was refluxed for four hours with azeotropic removal of water
- temperatureThe solution was cooled to 0° C.
- filtrationthe resulting crystals filtered (151.74 g, 54.95%)
- customRemoval of furan
Sources & evidence
- ORD record
- ord-3710d84d2a0043e5b0414d16ae327ec5
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855745B2
Reaction notes
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