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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62010Generated: October 29, 2026

Boron tribromide → HCID 136388719, compound

https://huagongshe.com/reaction/62010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant2-(5-(3,4-bis(benzyloxy)-5-nitrophenyl)-2H-tetrazol-2-yl)-5-(trifluoromethyl)pyridineHCID 68705633—
SolventDichloromethaneHCID 6344—
ProductHCID 136388719HCID 136388719—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446012B2
Source datasetuspto-grants-2016_09
ORD IDord-61386e057bbc45da8f82e50ff6871243
Source noteuspto-grants-2016_09