Reaktion #1929056

ord-fe1333c5e7414c1995d313ebd0cf237a

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 vacuum
  2. 2
    workup.DISSOLUTIONdissolved by addition of aqueous sodium hydroxide solution 1M (pH 10)
  3. 3
    Sonstigesubjected to dialysis
  4. 4
    Sonstigeagainst water hydrochloric acid 50 mM (1 L volume; 2 changes over 24 h) and water (1 L)

Vorschrift

A solution of freshly prepared 4-hydroxybenzoic acid (476 mg; 3.45 mmol) and BOP (1.7 g; 3.8 mmol) in DMF (20 mL) was added dropwise and at room temperature to a solution of PEI (1 g, 23.2 mmol) in DMF (30 mL). After 2 hours under stirring, the DMF was removed by evaporation under vacuum. The residue was taken in water (25 mL), dissolved by addition of aqueous sodium hydroxide solution 1M (pH 10) and subjected to dialysis using a SpectraPor 12-14 kDa membrane against water hydrochloric acid 50 mM (1 L volume; 2 changes over 24 h) and water (1 L). Lyophilization provided 4-hydroxybenzamide-PEI (1 g) at a modification degree of 13%. 1HNMR (D2O) δppm: 3.8-2.45 (m, 4H, NHCH2CH2NH), 6.9 (m, 0.25H, CHaro), 7.18 (m, 0.25H, CHaro).

Quelle

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