Reacción #730920

Ecuación de reacción

4-Oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-2-carboxylic acid

tert-butyl 2,2,2-trichloroacetimidate

Tert-butyl 2,2,2-trichloroacetimidate

tert-butyl 2,2,2-trichloroacetimidate

cyclohexane

→

title compound

Rendimiento 89.1%

4-Oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-2-carboxylic acid tert-butyl ester

Rendimiento 89.1%

Disolventes

dichloromethane

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGStirring
2. 2
   workup.WAITwas continued overnight
3. 3
   Otrowas quenched by cautious addition of solid NaHCO3 (˜1 g)
4. 4
   workup.ADDITIONSilica was added (˜80 mL)
5. 5
   Concentraciónthe resulting suspension was concentrated under reduced pressure
6. 6
   OtroThe resulting crude mixture was purified by silica gel chromatography (20% EtOAc in hexanes on 1 L of silica)

Procedimiento

4-Oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-2-carboxylic acid (Behringer, H.; Falkenberg, K. Chem. Ber., 1966, 99, 3309) (7.69 g, 39.19 mmol) was suspended in 120 mL 2:1 cyclohexane: dichloromethane. Tert-butyl 2,2,2-trichloroacetimidate (17.13 g, 78.38 mmol) was added in one portion, followed by boron trifluoride diethyl etherate (87.8 mg, 6.19 μmol, 0.16 mol %). The resultant slurry was stirred vigorously for 1.5 hours and a further portion of tert-butyl 2,2,2-trichloroacetimidate (8.57 g, 39.19 mmol) was added. Stirring was continued overnight. Further portions of tert-butyl 2,2,2-trichloroacetimidate (8.57 g, 39.19 mmol) were added at 1.5 hours and 3 hours and after a further 3 hours the reaction was quenched by cautious addition of solid NaHCO3 (˜1 g). Silica was added (˜80 mL) and the resulting suspension was concentrated under reduced pressure. The resulting crude mixture was purified by silica gel chromatography (20% EtOAc in hexanes on 1 L of silica) to afford the title compound as a light yellow solid (8.81 g, 89% yield). ). MS (ES+) 253. δH (CDCl3) 1.5-1.6 (9H, s), 2.2-2.3 (2H, m), 2.5-2.6 (2H, m), 3.0-3.1 (2H, m), 7.9 (1H, s).

Fuente