反応 #595372

ord-b6f5f043948143d59c16cb465ffc0948

反応方程式

COc1c(F)ccc(F)c1C(=O)O
3,6-difluoro-2-methoxybenzoic acid
CC(C)[N-]C(C)C.[Li+]
LDA
CC(C)NC(C)C
diisopropylamine
[Li][CH2]CCC
n-BuLi
CCOB(OCC)OCC
B(OEt)3
O=S(=O)(O)O
H2SO4
COc1c(F)c(B(O)O)cc(F)c1C(=O)O
title compound
COc1c(F)c(B(O)O)cc(F)c1C(=O)O
4-borono-3,6-difluoro-2-methoxybenzoic acid

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The organic phase was separated
  2. 2
    抽出the aqueous layer was extracted with Et2O
  3. 3
    濃縮The combined organics were concentrated
  4. 4
    洗浄the residue solid was washed with H2O and hexane
  5. 5
    その他dried

実験手順

To a solution of 3,6-difluoro-2-methoxybenzoic acid (i-6b) (0.94 g, 5 mmol) in THF (5 mL) at −70° C. was added a solution of LDA [freshly prepared from diisopropylamine (1.51 g, 15 mmol) and n-BuLi (10M solution in hexane, 1.5 mL, 15 mol) in THF (15 mL). The resultant solution was stirred for 15 mins, followed by the addition of B(OEt)3 (1.46 g, 10 mmol). The mixture was stirred for 15 mins and then hydrolyzed with dilute aq. H2SO4. The organic phase was separated and the aqueous layer was extracted with Et2O. The combined organics were concentrated and the residue solid was washed with H2O and hexane, dried to give the title compound as white crystals. LCMS (ESI) calc'd for C8H7BF2O5 [M+H]+: 233. found: 233.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09095583B2uspto-grants-2015_08