Reacción #833528

ord-25db0730452943b98863a06bede34555

Ecuación de reacción

CCC1(CO)COC1
3-ethyl-3-hydroxymethyloxetane
c1ccncc1
pyridine
Cc1ccc(S(=O)(=O)Cl)cc1
p-Toluene sulfonyl chloride
CCC1(COS(=O)(=O)c2ccc(C)cc2)COC1
3-[(tosyloxy)methyl]3-ethyloxetane

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGAfter stirring for 5 hours
  2. 2
    Otrowhile keeping at 0° C.
  3. 3
    ExtracciónIt was extracted with diethyl ether (500 mL)
  4. 4
    Lavadowere washed with water
  5. 5
    LavadoThen, the extracts were washed with a saturated solution of sodium carbonate and water successively
  6. 6
    Secadodried over anhydrous magnesium sulfate
  7. 7
    workup.DISTILLATIONThe solvent was distilled off

Procedimiento

3-ethyl-3-hydroxymethyloxetane (trade name of product, OXT-101®, manufactured by To a Gosei Co.; 116 g) was added to pyridine (500 mL) and cooled to 0° C. while stirring. p-Toluene sulfonyl chloride (190 g) was added divisionally for several times. After stirring for 5 hours while keeping at 0° C., the reaction mixture was poured to iced water (1 L). It was extracted with diethyl ether (500 mL), the pH was rendered acidic with 3% hydrochloric acid, and extracts were washed with water. Then, the extracts were washed with a saturated solution of sodium carbonate and water successively and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 3-[(tosyloxy)methyl]3-ethyloxetane (243 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07393569B2uspto-grants-2008_07