Reaction #1929057

ord-1123e1cfa31346568212ddbfce7260de

Reaction equation

O=C(O)c1ccc(O)cc1
4-hydroxybenzoic acid
CN(C)[P+](On1nnc2ccccc21)(N(C)C)N(C)C.F[P-](F)(F)(F)(F)F
BOP
NC(=O)c1ccc(O)cc1
4-hydroxybenzamide

Reagents

None

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherthe DMF was removed by evaporation under reduced pressure
  2. 2
    workup.DISSOLUTIONdissolved by addition of aqueous sodium hydroxide solution 1M (pH 11)
  3. 3
    Othersubjected to dialysis
  4. 4
    Otheragainst water (1 L, 2 changes over 24 h)

Procedure

A solution of freshly prepared 4-hydroxybenzoic acid (635 mg; 4.6 mmol) and BOP (1.7 g; 5.06 mmol) in DMF (20 mL) was added dropwise and at room temperature to a solution of PEI (1 g, 23.2 mmol) in DMF (50 mL). After 2 hours under stirring, the DMF was removed by evaporation under reduced pressure. The crude product was taken in water, dissolved by addition of aqueous sodium hydroxide solution 1M (pH 11) and subjected to dialysis using a SpectraPor 12-14 kDa membrane against water (1 L, 2 changes over 24 h). Lyophilization provided 4-hydroxybenzamide-PEI (0.7 g) at a modification degree of 28%. 1H NMR (D2O) δppm: 2.6 (bm, 2.9H, —NHCH2CH2NH—), 3.22 (m, 0.55H, Phe-CONHCH2CH2NH—), 3.35 (m, 0.55H, Phe-CONHCH2CH2NH) 6.57 (d, J=7.3 Hz, 0.55 H, CHaro), 6.97 (m, 0.55H, CHaro).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08945927B2uspto-grants-2015_02