تفاعل #88834

ord-f457df4c287242d89060fb6b3d20cb8d

معادلة التفاعل

COC(=O)c1ccc(Br)cc1Cl
4-bromo-2-chlorobenzoic acid methyl ester
C=[CH][Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC
tributyl(vinyl)tin
C=Cc1ccc(C(=O)O)c(Cl)c1
2-chloro-4-vinylbenzoic acid

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe crude reaction mixture
  2. 2
    تركيزwas then concentrated down
  3. 3
    ترشيحfiltered through a pad of celite
  4. 4
    تركيزconcentrated down

الإجراء التجريبي

To a solution of 4-bromo-2-chlorobenzoic acid methyl ester (500 mg, 2 mmol) in THF (15 mL) was added tributyl(vinyl)tin (620 μl, 2.1 mmol) and PdCl2(dppf)-2-DCM (165 mg, 0.2 mmol). The solution was heated to 60° C. for 12 hours. The crude reaction mixture was then concentrated down and taken up in 20 mL EtOAc and 100 mL concentrated KF solution. The reaction stirred at room temperature for 3 hours, filtered through a pad of celite and concentrated down. The residual oil was subjected to flash chromatography (Isco Companion, 40 g SiO2 cartridge, solid loaded SiO2, neat heptanes to EtOAc gradient) to give 2-chloro-4-vinylbenzoic acid as a yellow oil. Amount obtained: 235 mg (60%). LCMS (M/Z): 197 (M+H). 1H NMR (Chloroform-d) δ: 3.93 (s, 3 H) 5.42 (d, J=10.9 Hz, 1 H) 5.86 (d, J=17.6 Hz, 1 H) 6.66 (dd, J=17.6, 10.7 Hz, 1 H) 7.28-7.35 (m, 1 H) 7.43-7.50 (m, 1 H) 7.82 (d, J=8.0 Hz, 1 H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09440994B2uspto-grants-2016_09