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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916084Generated: October 30, 2026

Tetrahydrofuran → HCID 69457443, compound

https://huagongshe.com/reaction/916084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantBenzoic acid, 2-(bromomethyl)-, 1,1-dimethylethyl esterHCID 11459925—
ReactantHCID 69456394HCID 69456394—
SolventWaterHCID 962—
ProductHCID 69457443HCID 6945744371%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydride (104 mg, 2.86 mmol) and tetrahydrofuran (16 ml) were added to a previously dried reaction vessel. To the mixture were added 2-(benzimidazole-2-ylthiomethyl)benzoic acid methyl ester (428 mg, 1.43 mmol) and 2-(bromomethyl)benzoic acid t-butyl ester (466 mg, 3.46 mmol), and then the mixture was stirred at 60° C. for 50 minutes. Water was added thereto, followed by extraction with ethyl acetate. After the ethyl acetate phase was dried with anhydrous sodium sulfate, it was concentrated, and the residue was purified by silica gel column chromatography (hexane: ethyl acetate=3:1) to obtain 2-((1-((2-((t-butyl)oxycarbonyl)phenyl)methyl)benzimidazole-2-ylthio)methyl)benzoic acid methyl ester (495 mg, yield 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268145B2
Source datasetuspto-grants-2007_09
ORD IDord-7a50594bf5f04aee9226b1bb558c5956
Source noteuspto-grants-2007_09