Methyl 2-(3-bromophenyl)acetate → HCID 51035096, compound

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Reaction Steps

The title compound was prepared in analogy to Example 1 starting from (3-bromo-phenyl)-acetic acid methyl ester (commercially available) and 3-[1-phenyl-eth-(E)-ylidene]-1,3-dihydro-indol-2-one. 1H NMR (400 MHz, DMSO-d6) δppm 2.77 (s, 3H) 3.65 (s, 3H) 3.81 (s, 2H) 6.08 (d, J=7.33 Hz, 1H) 6.66-6.72 (m, 2H) 7.11 (t, J=7.33 Hz, 1H) 7.35-7.44 (m, 5H) 7.51-7.61 (m, 4H).

Provenance & Evidence