Réaction #77857

Équation de réaction

N-bromosuccimide

3,4-dihydro-2H-pyran

acetic acid

→

2-acetoxy-3-bromo-tetrahydropyran

Rendement 73.0%

Solvants

diethyl ether

Conditions de réaction

Traitement

1. 1
   Lavagewashed with 50 ml of water three times
2. 2
   LavageThe organic layer was washed with 1N NaHCO3 solution
3. 3
   Autredried
4. 4
   Concentrationconcentrated under a reduced pressure

Mode opératoire

To the solution of N-bromosuccimide (4.5 g ) in acetic acid (14.5 ml), was added dropwise 2.3 ml of 3,4-dihydro-2H-pyran at 10° C. The reaction mixture was diluted with 50 ml of diethyl ether and washed with 50 ml of water three times. The organic layer was washed with 1N NaHCO3 solution, dried, and then concentrated under a reduced pressure to give 4.1 g of 2-acetoxy-3-bromo-tetrahydropyran as a colorless oil (yield: 73%).

Source