反应 #595372

ord-b6f5f043948143d59c16cb465ffc0948

反应方程式

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

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The organic phase was separated
  2. 2
    萃取the aqueous layer was extracted with Et2O
  3. 3
    浓缩The combined organics were concentrated
  4. 4
    洗涤the residue solid was washed with H2O and hexane
  5. 5
    其他dried

实验过程

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.

来源

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