Réaction #1244273

ord-8c5c1fd2fa0d4b75a13eb54c448fa0f9

Équation de réaction

OC1COC(c2ccccc2)OC1
2-phenyl-1,3-dioxan-5-ol
CCN(CC)CC
triethyl amine
Cc1ccc(S(=O)(=O)Cl)cc1
tosyl chloride
Cc1ccc(S(=O)(=O)OC2COC(c3ccccc3)OC2)cc1
white solid
Rendement 96.0%
Cc1ccc(S(=O)(=O)OC2COC(c3ccccc3)OC2)cc1
2-Phenyl-1,3-dioxan-5-yl 4-methylbenzenesulfonate
Rendement 96.0%

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONThe reaction was poured onto water (800 mL)
  2. 2
    Extractionextracted into DCM
  3. 3
    Concentrationconcentrated to dryness
  4. 4
    AutreThe crude mixture was recrystallized from EtOAc

Mode opératoire

To a 2 liter round bottom flask was added 2-phenyl-1,3-dioxan-5-ol (50 g, 277 mmol), triethyl amine (42.1 g, 416 mmol), DMAP (3.39 g, 27.7 mmol) and dichloromethane (1 L). The reaction was cooled to 0° C. To this solution was added tosyl chloride (58.2 g, 305 mmol) and the reaction was stirred overnight at RT. The reaction was poured onto water (800 mL) and extracted into DCM. The organic layers were combined and concentrated to dryness. The crude mixture was recrystallized from EtOAc:Hex to afford 88 g (96% yield) of a white solid. 1H NMR (CDCl3, 400 MHz), δ: 2.44 (3H, s), 4.09 (2H, dd, J=13.6, 2 Hz), 4.27 (2H, dd, J=13.6, 1.6 Hz), 4.51 (2H, pseudo t, J=1.6 Hz), 7.33-7.36 (5H, m), 7.44-7.45 (2H, m), 7.85 (2H, d, J=8.39 Hz). Mass Spec (lo-res): Calc'd for C17H18O5S: 334.09. found: 335.1 (M+H).

Source

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