反応 #435498

ord-e81c15bfd0d845bbacee3f16f0299fc0

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe mixture was stirred vigorously
  2. 2
    その他The solution was partitioned
  3. 3
    洗浄the organic layer was washed twice with water and brine
  4. 4
    乾燥dried over Na2SO4
  5. 5
    濃縮concentrated in vacuo

実験手順

3-(4-Benzyloxyphenyl)-3-hydroxy-2-(2-fluorophenoxy)-2-methylpropionic acid ethyl ester (9.5 mmol) in anhydrous CH2Cl2 (30 mL) was cooled to 0° C. and treated with BF3-Et2O (1.16 mL, 9.5 mmol) and triethylsilane (1.51 mL, 9.5 mmol). The mixture was stirred for 2 h and gradually warmed to ambient temperature. Saturated aqueous Na2CO3 (15 mL) was added and the mixture was stirred vigorously. The solution was partitioned and the organic layer was washed twice with water and brine, dried over Na2SO4, and concentrated in vacuo to produce 3-(4-benzyloxyphenyl)-2-(2-fluorophenoxy)-2-methylpropionic acid ethyl ester as an oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07176224B2uspto-grants-2007_02