Reacción #335039

Ecuación de reacción

5-hexynoic acid

N-bromosuccinimide

tetrabutylammonium hydroxide

→

product

Rendimiento 58.0%

(E)-6-(Bromomethylene)tetrahydro-2H-pyran-2-one

Rendimiento 58.0%

Disolventes

CH2Cl2

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThis compound was prepared
2. 2
   LavadoThe mixture was washed with 5% Na2S2O3 and saturated NaCl
3. 3
   SecadoThe organic phase was dried (MgSO4)
4. 4
   Otrothe solvent was removed in vacuo
5. 5
   Otroto give a residue
6. 6
   OtroThe residue was purified by flash chromatography (silica gel, Aldrich catalog #22,719-6, 230-400 mesh)
7. 7
   LavadoThe column was eluted with CH2Cl2 and fractions
8. 8
   OtroThe solvent was removed in vacuo

Procedimiento

This compound was prepared according to the procedure set forth in Kraft et al, J. Am. Chem. Soc., 103, 5459-5466 (1981). A mixture of the 5-hexynoic acid of Part A (1.1 g, 9.8 mmol), KHCO3 (1.5 g, 15 mmol), N-bromosuccinimide (2.6 g, 15 mmol) and 0.4M aqueous tetrabutylammonium hydroxide (2 mL, 0.8 mmol) in CH2Cl2 (90 mL) was stirred at room temperature for 3.5 h. The mixture was washed with 5% Na2S2O3 and saturated NaCl. The organic phase was dried (MgSO4) and the solvent was removed in vacuo to give a residue weighing 1.8 g. The residue was purified by flash chromatography (silica gel, Aldrich catalog #22,719-6, 230-400 mesh). The column was eluted with CH2Cl2 and fractions having a spot with Rf =0.32 (CH2Cl2, Bakerflex IBF-2 silica TLC plates) were combined. The solvent was removed in vacuo to give 1.0 g (58% yield) of product as a colorless oil.

Fuente