Reacción #1137869

Ecuación de reacción

n-BuLi

hexane

2,3-dihydrothieno[3,4-b][1,4]dioxine

tetramethylethylenediamine

Tributylstannyl chloride

→

tributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannane

Rendimiento 40.0%

Disolventes

tetrahydrofuran

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturacooled in a dry ice/acetone bath
2. 2
   workup.STIRRINGstirred at this temperature for 1 hour
3. 3
   Temperaturacooled in a dry ice/acetone bath
4. 4
   Temperaturato warm up
5. 5
   OtroThe volatiles were removed under reduced pressure
6. 6
   workup.ADDITIONThe residue was diluted with toluene (100 mL)
7. 7
   Otrochromatographed
8. 8
   workup.ADDITIONfilled with silica gel (500 mL)
9. 9
   Lavadowashed with 2% triethylamine in hexane (500 mL)

Procedimiento

1.5M n-BuLi in hexane (53 mL, 80 mmol) was added in small portions to a solution of 2,3-dihydrothieno[3,4-b][1,4]dioxine (10.00 g, 80 mmol) and tetramethylethylenediamine (12.0 mL, 80 mmol) in tetrahydrofuran (100 mL) stirred under argon and cooled in a dry ice/acetone bath. The reaction mixture was heated to 35° C., stirred at this temperature for 1 hour, and then cooled in a dry ice/acetone bath. Tributylstannyl chloride (20.3 mL), 75 mmol was then added, the mixture was allowed to warm up, and it was left at room temperature for 16 hours. The volatiles were removed under reduced pressure. The residue was diluted with toluene (100 mL) and chromatographed using a column filled with silica gel (500 mL) washed with 2% triethylamine in hexane (500 mL) to give tributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannane (12.17 g, 40%) of high purity. 1H NMR (400 MHz, CDCl3): δ 6.57 (s, 1H, thiophene), 4.15 (m, 4H, OCH2CH2O), 1.53 (m, 6H, Bu), 1.32 (quintet, J=7.3 Hz, 6H, Bu), 1.09 (m, 6H, Bu), 0.88 (t, J=7.3 Hz, 9H, Bu).

Fuente