반응 #10739

ord-8369248867f0408eb05df10e2fc0ea3b

반응 방정식

OB(O)c1cccs1
Thiophene-2-boronic acid
O=P([O-])([O-])[O-].[K+].[K+].[K+]
potassium phosphate
COc1ccc(C=O)c(OS(=O)(=O)C(F)(F)F)c1
trifluoro-methanesulfonic acid 2-formyl-5-methoxy-phenyl ester
COc1ccc(C=O)c(-c2cccs2)c1
4-methoxy-2-thiophen-2-yl-benzaldehyde
수율 90.0%

반응 조건

온도
95°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도Upon cooling to room temperature the reaction
  2. 2
    농축The organic phase was concentrated under reduced pressure

실험 절차

Ex-34B: A solution of trifluoro-methanesulfonic acid 2-formyl-5-methoxy-phenyl ester (Ex-34A, 1.6 g, 5.63 mmol) in 1,4-dioxane (15 mL) was stirred at room temperature under nitrogen for 5 min. Thiophene-2-boronic acid (1.08 g, 8.44 mmol), tetrakis(triphenylphosphine)palladium(0) (0.65 g, 0.56 mmol) and a potassium phosphate (2.2 g, 10.36 mmol) were then added and the resulting mixture was heated to 95° C. under nitrogen overnight. Upon cooling to room temperature the reaction was diluted with EtOAc (25 mL) and water (25 mL) and the layers were cut. The organic phase was concentrated under reduced pressure. Silica gel chromatography (hexane/ethyl acetate, 4:1) gave 1.1 g (90%) of the desired 4-methoxy-2-thiophen-2-yl-benzaldehyde product. 1H-NMR (300 MHz, CDCl3): 10.06 (s, 1H), 8.03 (m, 1H), 7.45 (m, 1H), 7.14 (m, 1H), 7.09 (m, 1H), 7.00 (m, 2H), 3.91 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07094801B2uspto-grants-2006_08