HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62010Generated: October 29, 2026
Boron tribromide → HCID 136388719, compound
https://huagongshe.com/reaction/62010
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(5-(3,4-bis(benzyloxy)-5-nitrophenyl)-2H-tetrazol-2-yl)-5-(trifluoromethyl)pyridine | HCID 68705633 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136388719 | HCID 136388719 | — |
Reaction Steps
A solution of 2-(5-(3,4-bis(benzyloxy)-5-nitrophenyl)-2H-tetrazol-2-yl)-5-(trifluoromethyl)pyridine (0.274 g, 0.5 mmol) in dichloromethane (15 mL) was cooled to −78° C. with stirring under argon and treated with boron tribromide (1.00 g, 4.00 mmol) dropwise. The resulting deep purple suspension was then allowed to stir at room temperature for one hour before cooling again to −78° C. The mixture was quenched by the careful addition of methanol. After stirring at room temperature for thirty minutes, the volatiles were evaporated and the residue stirred with 2 N hydrochloric acid (5 mL) for thirty minutes. The resulting solid was filtered off, washed with water (25 mL) and then cold isopropanol (5 mL) to give 3-nitro-5-(2-(5-(trifluoromethyl)pyridin-2-yl)-2H-tetrazol-5-yl)benzene-1,2-diol as a yellow solid, 0.165 g, (90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09446012B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-61386e057bbc45da8f82e50ff6871243 |
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| Source note | uspto-grants-2016_09 |
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