Reaktion #1929058

ord-7b403af834664796bea865e9fdeabcb0

Reaktionsgleichung

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

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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 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, 0.55H, CHaro), 6.97 (m, 0.55H, CHaro).

Quelle

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