Syntheses of amorfrutin C, a natural product with potent antitumor activity, as well as pseudo‐amorfrutin A were accomplished. Protected 2,4‐dihydroxybenzoic acid derivative 5 was used as a common synthetic intermediate. The introduction of a prenyl moiety to 5 was achieved through bromination followed by a CuCN‐meditated alkylation reaction. Interestingly, N‐bromosuccinimide promoted monobromination at the 6‐position, leading to pseudo‐amorfrutin A; 1,3‐dibromo‐5,5‐dimethylhydantoin triggered bromination at both the 6‐ and 8‐positions, leading to naturally occurring amorfrutin C.