HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916084Generated: October 30, 2026
Tetrahydrofuran → HCID 69457443, compound
https://huagongshe.com/reaction/916084
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzoic acid, 2-(bromomethyl)-, 1,1-dimethylethyl ester | HCID 11459925 | — |
| Reactant | HCID 69456394 | HCID 69456394 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69457443 | HCID 69457443 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268145B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-7a50594bf5f04aee9226b1bb558c5956 |
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| Source note | uspto-grants-2007_09 |
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