Synthesis　of　a　Ti-incorporated　zeolite　using　a　simple　and　economical　method　has　recently　become　a　focus　of　attention.　The　direct　hydrothermal　synthesis　of　Ti-MWW　is　most　commonly　applied;　however,　it　is　challenging　to　perform　and　exhibits　low　titanium　utilization.　An　innovative　strategy　of　synthesizing　Ti-MWW　is　proposed　in　the　present　study　by　simply　treating　the　ERB-1　precursor　of　an　MWW-type　boron　silicate　with　a　H2TiF6/HNO3　solution.　This　significantly　shortens　the　Ti　grafting　process　from　5　days　to　only　a　few　hours　and　reduces　the　use　of　the　structure-directing　agent　hexamethyleneimine　(HMI);　furthermore,　no　extraframework　Ti　is　observed　in　the　precursor,　indicating　good　atomic　economy.　Typically,　a　piperidine　(PI)-treated　sample　Ti-MWW2-1-PI　exhibits　a　higher　conversion　(76.6%)　than　the　original　Ti-MWW　(44.8%)　in　the　epoxidation　of　1-hexene.　X-ray　diffraction　(XRD),　inductively　coupled　plasma　(ICP),　and　transmission　electron　microscopy　(TEM)　techniques　are　used　to　explain　in　detail　the　probable　mechanism　underlying　the　incorporation　of　Ti　species　into　the　MWW　framework.　X-ray　photoelectron　spectroscopy　(XPS)　is　employed　to　study　the　coordinate　state　of　the　Ti　and　F　species　in　the　samples　after　treatment　with　a　piperidine　solution.　This　method　can　be　applied　to　synthesize　other　kinds　of　lamellar-structured　zeolites　with　heteroatoms.　Copyright　©　2020　American　Chemical　Society.