Réaction #1244275

ord-b41c88cbe3064d109a238904d26ca606

Équation de réaction

O
water
CCOC(C)=O
EtOAc
CCOC(C)=O
EtOAc
CCC(CC)(CC)C([O-])([O-])[O-]
triethylorthoacetate
[N-]=[N+]=NC(CO)CO
2-Azidopropane-1,3-diol
CC(=O)OCC(CO)N=[N+]=[N-]
24
Rendement 57.3%
CC(=O)OCC(CO)N=[N+]=[N-]
2-Azido-3-hydroxypropyl acetate
Rendement 57.3%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Concentrationconcentrated in vacuo
  2. 2
    AutrePurification of the residue on a silica gel cartridge

Mode opératoire

2-Azidopropane-1,3-diol 23 (10.46 g, 89.3 mmol) was dissolved in CH2Cl2 (450 mL) and treated with a catalytic amount of p-toluene sulfonic acid monohydrate (340 mg, 1.8 mmol) and triethylorthoacetate (24.4 mL, 134 mmol) at room temperature for 1 hr. After the formation of the orthoester was complete, a stoichiometric amount of water (2.4 mL, 134 mmol) was added to the mixture. The mixture was then stirred for 40 min and then concentrated in vacuo. Purification of the residue on a silica gel cartridge using EtOAc:Hex as the eluent (5% EtOAc to 100% EtOAc) afforded 8.14 g (57% yield) of 24 as a clear, colorless oil. 1H NMR (CDCl3, 400 MHz), δ: 2.45 (1H, br s), 2.12 (3H, s), 3.63-3.78 (3H, m), 4.20-4.30 (2H, m).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07807394B2uspto-grants-2010_10