Reaktion #480052

Reaktionsgleichung

triethyl borate

butyl lithium

5-benzyloxy-2-bromo-4-ethyl-1-methoxybenzene

→

4-benzyloxy-5-ethyl-2-methoxy-phenylboronic acid

Ausbeute 71.6%

Lösungsmittel

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwhile maintaining the temperature below −70° C
2. 2
   workup.STIRRINGto stir at −78° C. for an additional 2 hours
3. 3
   Temperaturto warm to 23° C. over a 30 minute period
4. 4
   Sonstigewas quenched with 100 mL of saturated NH4Cl
5. 5
   Extraktionthe resultant solution was extracted with ethyl acetate (2×200 mL)
6. 6
   WaschenThe combined extracts were washed with brine (1×100 mL)
7. 7
   Trocknendried over sodium sulfate
8. 8
   Filtrationfiltered
9. 9
   Einengenconcentrated in vacuo
10. 10
    Sonstigeto yield crude product as a greenish-tan solid
11. 11
    SonstigeThe crude product was triturated with hexane
12. 12
    Filtrationfiltered

Vorschrift

Under a nitrogen atmosphere, 16.70 g (52.00 mmol) of 5-benzyloxy-2-bromo-4-ethyl-1-methoxybenzene (4) was added to 110 mL of anhydrous THF. The solution was cooled to −78° C., and 22.88 mL (57.19 mmol) of a 2.5 M solution of butyl lithium was added dropwise while maintaining the temperature below −70° C. The reaction mixture was stirred at −78° C. for 45 minutes. 9.73 mL (57.19 mmol) of triethyl borate was then added, and the reaction was allowed to stir at −78° C. for an additional 2 hours. The reaction mixture was then allowed to warm to 23° C. over a 30 minute period and was quenched with 100 mL of saturated NH4Cl. The pH was adjusted to 5.0 with 1M HCl, and the resultant solution was extracted with ethyl acetate (2×200 mL). The combined extracts were washed with brine (1×100 mL), dried over sodium sulfate, filtered and concentrated in vacuo to yield crude product as a greenish-tan solid. The crude product was triturated with hexane and filtered to afford 10.65 g (64%) of 4-benzyloxy-5-ethyl-2-methoxy-phenylboronic acid (5) as an off-white solid.

Quelle