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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573274Generated: October 29, 2026

Water → [4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl](1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazol-2-yl)methanone

https://huagongshe.com/reaction/573274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-benzo[D]imidazoleHCID 10922907—
ReactantN-methoxy-N-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamideHCID 46739065—
SolventTetrahydrofuranHCID 8028—
Product[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl](1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazol-2-yl)methanoneHCID 8668895953.1%

Reaction Steps

To a solution of 1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzo[d]imidazole (6.06 g) in THF (50 mL) was added LiHMDS (1 M solution in THF, 30 ml) dropwise at 0° C. After stirring for 1 h, a solution of N-methoxy-N-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (7.10 g) in THF (50 mL) was added dropwise, and the mixture was stirred for 1 h at 0° C. The reaction mixture was poured into water and extracted with AcOEt. The extract was washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/AcOEt) and crystallized from hexane to give the title compound (6.20 g). 1H NMR (300 MHz, CDCl3) δ −0.11 (9H, s), 0.84-0.91 (2H, m), 1.37 (12H, s), 3.55-3.62 (2H, m), 6.03 (2H, s), 7.37-7.43 (1H, m), 7.45-7.50 (1H, m), 7.65-7.70 (1H, m), 7.91-7.98 (3H, m), 8.22-8.26 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029536B2
Source datasetuspto-grants-2015_05
ORD IDord-28bfb01709c94763a4961172e640c3da
Source noteuspto-grants-2015_05