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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42665Generated: October 30, 2026

Boron tribromide → HCID 136388719, compound

https://huagongshe.com/reaction/42665

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 numberUS08536203B2
Source datasetuspto-grants-2013_09
ORD IDord-abdaf945375148b3bb5437435d36df8e
Source noteuspto-grants-2013_09