反応 #1929056

ord-fe1333c5e7414c1995d313ebd0cf237a

反応方程式

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

試薬

なし

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the DMF was removed by evaporation under vacuum
  2. 2
    workup.DISSOLUTIONdissolved by addition of aqueous sodium hydroxide solution 1M (pH 10)
  3. 3
    その他subjected to dialysis
  4. 4
    その他against water hydrochloric acid 50 mM (1 L volume; 2 changes over 24 h) and water (1 L)

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08945927B2uspto-grants-2015_02