Reacción #1914818

ord-4f40d148a78a4ee4aa17aa0d13fc831b

Ecuación de reacción

O=C(O)c1sc(C(=O)O)c2c1OCC(CO)O2
2-Hydroxymethyl-2,3-dihydro-thieno[3,4-b][1,4]dioxine-5,7-dicarboxylic acid
CCOC(C)=O
ethyl acetate
OCC1COc2cscc2O1
(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-yl)-methanol

Condiciones de reacción

Temperatura
150°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaafter which it was cooled to 25° C
  2. 2
    Otrothe catalyst was removed by filtration
  3. 3
    Lavadothe filtrate was washed with acidic water
  4. 4
    OtroSubsequently, the solvent was removed after which pure (2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-yl)-methanol
  5. 5
    Otrowas isolated by vacuum distillation (115–120° C.; 0.05 mm Hg)

Procedimiento

2-Hydroxymethyl-2,3-dihydro-thieno[3,4-b][1,4]dioxine-5,7-dicarboxylic acid (48 g, 0.184 mol) was dissolved in N,N-dimethylacetamide (500 mL), and Cu2Cr2O7 (8.6 g) and quinoline (15 drops) were added. This mixture was subsequently stirred for 2 hours at 150° C., after which it was cooled to 25° C. It was then poured into ethyl acetate, the catalyst was removed by filtration and the filtrate was washed with acidic water and aqueous, saturated NaCl. Subsequently, the solvent was removed after which pure (2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-yl)-methanol was isolated by vacuum distillation (115–120° C.; 0.05 mm Hg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07056600B2uspto-grants-2006_06