Reaction #1442490

ord-697730dd1f5743999dd5e53ecfb10324

Reaction equation

[Br-].[K+]
KBr
NCCNCCNCCN
Triethylene tetramine
C=C(C)C(=O)Cl
methacryloyl chloride
C=C(C)C(=O)N(C(=O)C(=C)C)C(CNCCNCCN)(C(=O)C(=C)C)C(=O)C(=C)C
Tetra methacryloyl triethylene tetramine

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGThe reaction was continued stirring at room temperature overnight
  2. 2
    Otherthe suspension formed
  3. 3
    Filtrationwas filtered
  4. 4
    ExtractionThe filtrate was extracted with NaOH (aq)
  5. 5
    OtherThe water was rotary evaporated
  6. 6
    Washthe residue was washed with acetone
  7. 7
    Filtrationfiltered
  8. 8
    ConcentrationThe acetone filtrate was concentrated down
  9. 9
    Otherto obtain a white solid
  10. 10
    OtherThe solid is recrystallized from diethyl ether
  11. 11
    Otherto give white crystals, m.p. 168-170° C

Procedure

Triethylene tetramine (2.93 g, 0.02 moles) in dichloromethane (100 ml) was added drop wise over 6 hrs to a solution of methacryloyl chloride (8.32 g, 0.08 moles) in dichloromethane (40 ml), stirring vigorously at room temperature. The reaction was continued stirring at room temperature overnight and the suspension formed was filtered. The filtrate was extracted with NaOH (aq). The water was rotary evaporated and the residue was washed with acetone and filtered. The acetone filtrate was concentrated down and put through a silica gravity chromatography column with acetone as the elutant to obtain a white solid. The solid is recrystallized from diethyl ether to give white crystals, m.p. 168-170° C. 1H n.m.r. (D2O) δ, 5.71(19.7 Hz), 5.51 (7.8 Hz), 5.31(9.7 Hz), 5.06 (17.7 Hz), (8 H, d×4) C—CH2; 3.61 (6 H, m) N—CH2—CH2; 3.48(6 H, m) N—CH2—CH2; 1.96(4.1 Hz); 1.93(5.8 Hz); 1.91(6.0 Hz); 1.88(4.5 Hz), (12 H, d×4) CH3; 13C n.m.r. (D2O), δ 178.76, 178.70, 174.71, 174.61 (C=O); 142.19, 142.0, 141.71, 141.56 (C=CH2), 124.52, 124.19, 120.06, 119.60 (C=CH2); 22.30, 22.20, 20.48; (CH3), 50.33, 49.22, 46.45, 44.00, 40.22, 39.49 (N—CH2—CH2). MS: mz: 419.3 (MH+, 100%), 391.3(4), 266.2(10), 223.1(42); HRMS: found: 419.26695 C22H34N4O4 requires 418.5299. Elemental analysis: found: C, 62.97; H, 8.09; N, 13.31; C22H34N4O4 requires C, 63.13; H, 8.19; N, 13.39. I.R. (KBr) (CM−1) 3353, 1665, 1650, 1530, 1279.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06585873B1uspto-grants-2003_07