Reaktion #53541

ord-a263a6c6aab24b52ae051db78b79b634

Reaktionsgleichung

Nc1ccc(O)cc1
4-aminophenol
CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
di-tert-butyl-dicarbonate
CCN(C(C)C)C(C)C
diisopropylethylamine
CC(C)(C)OC(=O)c1ccc(O)c(N)c1
4Boc-aminophenol
Ausbeute 96.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenconcentrated
  2. 2
    Waschenthe solution was washed with brine
  3. 3
    Trocknendried (MgSO4)
  4. 4
    Einengenconcentrated
  5. 5
    SonstigePurification on a silica gel column
  6. 6
    Wascheneluting with 5% methanol/40% ethyl acetate hexane

Vorschrift

To a solution of 4-aminophenol (10.9 g, 100 mmol) in THF (150 mL) cooled in an ice bath was added di-tert-butyl-dicarbonate (21.8 g, 100 mmol) followed by diisopropylethylamine (17.4 mL, 100 mmol). The mixture was stirred at room temperature overnight and concentrated. The residue was taken up in ethyl acetate and the solution was washed with brine, dried (MgSO4), and concentrated. Purification on a silica gel column eluting with 5% methanol/40% ethyl acetate hexane gave 4Boc-aminophenol (20.1 g, 96%). MS(NH3—CI): (M+NH3+H)=227.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06858626B2uspto-grants-2005_02