Reacción #48331

Ecuación de reacción

3-(Benzyloxy)cyclobutanone Methylsulfinyl(methylthio)methane

n-Butyllithium

water

1-((1,3-dibromopropan-2-yloxy)methyl)benzene

→

3-(benzyloxy)cyclobutanone

Disolventes

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONwas added
2. 2
   TemperaturaThe mixture was cooled down to −78° C.
3. 3
   workup.STIRRINGThe reaction was stirred over night
4. 4
   Temperaturato warm up to RT
5. 5
   Extracciónextracted with EtOAc
6. 6
   OtroThe combined organic extracts were evaporated
7. 7
   workup.DISSOLUTIONdissolved in ether (50 ml)
8. 8
   workup.ADDITIONtreated with conc. HCl (10 ml) for 30 min
9. 9
   Temperaturaat reflux
10. 10
    Extracciónextracted with EtOAc
11. 11
    SecadoThe combined organic extracts were dried over MgSO4
12. 12
    Otroevaporated

Procedimiento

3-(Benzyloxy)cyclobutanone Methylsulfinyl(methylthio)methane (13 ml, 125 mmol) was dissolved in 250 ml THF and cooled to −20° C. n-Butyllithium (50 ml, 125 mmol) was added and the mixture was stirred for 3 h at −20° C. The mixture was cooled down to −78° C. and a solution of 1-((1,3-dibromopropan-2-yloxy)methyl)benzene (16.000 g, 52 mmol) was added. The reaction was stirred over night and allowed to warm up to RT. It was stirred for an additional 6h at RT, hydrolyzed with water and extracted with EtOAc. The combined organic extracts were evaporated, dissolved in ether (50 ml) and treated with conc. HCl (10 ml) for 30 min at reflux. The mixture was neutralized with NaOH (10M) and extracted with EtOAc. The combined organic extracts were dried over MgSO4 and evaporated. Glass col. Chrom. (10-50% EtOAc in Hex) gave 3-(benzyloxy)cyclobutanone as a yellow oil.

Fuente