반응 #2006422

ord-f1ad1fc3e74643799d24f0bcdfe0d3aa

반응 방정식

O=Cc1cccc(C(=O)O)c1
3-carboxybenzaldehyde
C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
lithium bis(trimethylsilyl)amide
C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
lithium bis(trimethylsilyl) amide
[Br-].c1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1
benzyltriphenylphosphonium bromide
Cl
HCl
O=C(O)c1cccc(C=Cc2ccccc2)c1
title compound
수율 17.6%
O=C(O)c1cccc(C=Cc2ccccc2)c1
3-(2-Phenylethenyl)-benzoic Acid
수율 17.6%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출the separated aqueous layer was extracted with ethyl acetate (3×50 mL)
  2. 2
    건조dried (MgSO4 anh.)
  3. 3
    여과filtered
  4. 4
    기타evaporated
  5. 5
    기타The residue was purified by HPLC (10:95 CH3CN:H2O, TFA 0.1%)

실험 절차

A 1.0 M solution of lithium bis(trimethylsilyl) amide (3.3 mL, 3.3 mmol) in THF was added to a stirred suspension of benzyltriphenylphosphonium bromide (1.44 g, 3.6 mmol) in THF (35 mL) at 0° C. The resulting orange solution was added via cannula to a mixture of 3-carboxybenzaldehyde (500 mg, 3.3 mmol) and lithium bis(trimethylsilyl)amide (3.3 mL, 3.3 mmol) in THF (10 mL). The mixture was stirred overnight at room temperature. A 1N solution of HCl (75 mL) and ethyl acetate (75 mL) were added and the separated aqueous layer was extracted with ethyl acetate (3×50 mL), dried (MgSO4 anh.) filtered and evaporated. The residue was purified by HPLC (10:95 CH3CN:H2O, TFA 0.1%) to afford 130 mg of the title compound (17%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE043343E1uspto-grants-2012_05