Reacción #1495918

Ecuación de reacción

6-bromo-2′,4′,5′,6′-tetrahydrospiro[chroman-2,3′-pyran]-4-one

bis-trimethylsilylcarbodiimide

→

(E)-N-(6-bromo-2′,4′,5′,6′-tetrahydrospiro[chroman-2,3′-pyran]-4-ylide-ne)cyanamide

Rendimiento 90.0%

Disolventes

DCM

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONafter the addition
2. 2
   workup.STIRRINGThe resulting mixture was stirred for another 18 h
3. 3
   workup.ADDITIONafter the addition
4. 4
   Extracciónextracted with DCM (3×30 mL)
5. 5
   SecadoThe combined organic phases were dried over anhydrous Na2SO4
6. 6
   Filtraciónfiltered
7. 7
   ConcentraciónThe filtrate was concentrated

Procedimiento

To a solution of 6-bromo-2′,4′,5′,6′-tetrahydrospiro[chroman-2,3′-pyran]-4-one (379 mg, 1.28 mmol) in anhydrous DCM (10 mL) was added TiCl4 (1 M solution in DCM, 2.6 mL, 2.6 mmol) dropwise within 15 minutes at room temperature. The mixture was stirred another 1 h after the addition. To this mixture was added bis-trimethylsilylcarbodiimide (0.525 g, 0.63 mL, 2.82 mmol) dropwise. The resulting mixture was stirred for another 18 h after the addition. The reaction mixture was poured into ice-water (50 g) and extracted with DCM (3×30 mL). The combined organic phases were dried over anhydrous Na2SO4, and filtered. The filtrate was concentrated to give (E)-N-(6-bromo-2′,4′,5′,6′-tetrahydrospiro[chroman-2,3′-pyran]-4-ylide-ne)cyanamide (350 mg, 90%), which was used for next step without further purification.

Fuente