Reacción #1244441

ord-3d218947741c4a2fb1148d4eb5f50198

Disolventes

Condiciones de reacción

Temperatura
95°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAt this time, the reaction was poured onto water (200 mL)
  2. 2
    Extracciónextracted into methylene chloride (3×100 mL)
  3. 3
    LavadoThe organics were washed with water (1×100 mL)
  4. 4
    Secadoa saturated aqueous sodium chloride solution (1×100 mL), dried with magnesium sulfate
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated under vacuum

Procedimiento

A solution of dimethyl-thiocarbamic acid S-{4-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,6-dichloro-phenyl}ester (72) (2.0 g, 3.76 mmol) in ethanol (6.0 mL) was treated with a 3N aqueous potassium hydroxide solution (4.4 mL, 13.2 mmol). The reaction was then heated to 95° C. for 18 h. At this time, the reaction was poured onto water (200 mL), acidified to pH=2 with a 3N aqueous hydrochloric acid solution, and then extracted into methylene chloride (3×100 mL). The organics were washed with water (1×100 mL) and a saturated aqueous sodium chloride solution (1×100 mL), dried with magnesium sulfate, filtered, and concentrated under vacuum. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 80:20 petroleum ether/ethyl acetate) afforded 2-(3,5-dichloro-4-mercapto-phenyl)-ethanol (73) (639 mg, 76%) as a white solid; EI(+)-HRMS m/e calcd for C8H8Cl2OS (M+) 221.9673, found 221.9672. Exact Mass=221.9673; Molecular Weight=223.12

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07807674B2uspto-grants-2010_10