Réaction #42733

Équation de réaction

product

6-Bromoacetyl-2,2-dimethyl-4H-benzo[1,3]dioxine

BH3-THF

→

title compound

(R)-2-Bromo-1-(2,2-dimethyl-4H-benzo[1,3]dioxin-6-yl)ethanol

Solvants

THF

THF

Conditions de réaction

Traitement

1. 1
   Autrethe solid catalyst of Preparation 13, step (c)(1) (0.97 g, 3.5 mmol)
2. 2
   TempératureThe solution was cooled to between −20° C. and −10° C.
3. 3
   workup.ADDITIONwas added dropwise via a dropping funnel
4. 4
   workup.ADDITIONAfter the addition
5. 5
   Autrethe reaction mixture was quenched by slow addition of 50 mL of methanol
6. 6
   Concentrationconcentrated to a thick oil
7. 7
   AutreThe oil was purified by silica gel chromatography
8. 8
   Lavageeluted with 1:2 ethyl acetate/hexanes
9. 9
   Concentrationconcentrated

Mode opératoire

To the product of step (c) (10 g, 35.1 mmol) in 100 mL of THF was added the solid catalyst of Preparation 13, step (c)(1) (0.97 g, 3.5 mmol). The solution was cooled to between −20° C. and −10° C. and BH3-THF (35 mL, 35 mmol) diluted with 50 mL THF was added dropwise via a dropping funnel. After the addition was complete, the reaction mixture was allowed to warm to ambient temperature. After 30 minutes, the reaction mixture was quenched by slow addition of 50 mL of methanol and then concentrated to a thick oil. The oil was purified by silica gel chromatography eluted with 1:2 ethyl acetate/hexanes. The fractions were combined and concentrated to give the title compound as an off-white solid.

Source