반응 #464582

ord-17136e36bfcc45079fd2cbde0bc8509a

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타partitioned between 1.0 N HCl and EtOAc (300 mL each)
  2. 2
    기타The layers were separated
  3. 3
    건조the organic phase was dried over Na2SO4
  4. 4
    농축Concentration in vacuo
  5. 5
    기타produced a white solid
  6. 6
    기타that was triturated from Et2O/hexanes
  7. 7
    여과Filtration

실험 절차

To a solution of 6-methoxybenzo[b]thiophene (Graham, S. L., et al. J. Med. Chem. 1989, 32, 2548-2554)(18.13 g, 0.111 mol) in 150 mL of anhydrous THF at -60° C. was added n-BuLi (76.2 mL, 0.122 mol, 1.6 M solution in hexanes), dropwise via syringe. After stirring for 30 min, triisopropyl borate (28.2 mL, 0.122 mol) was introduced via syringe. The resulting mixture was allowed to gradually warm to 0° C. and then partitioned between 1.0 N HCl and EtOAc (300 mL each). The layers were separated, and the organic phase was dried over Na2SO4. Concentration in vacuo produced a white solid that was triturated from Et2O/hexanes. Filtration provided 16.4 g (71%) of 6-methoxybenzo[b]thiophene-2-boronic acid as a white solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06025382uspto-grants-2000_02