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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369037Generated: October 26, 2026

Triethyl borate → B-2,1,3-Benzoxadiazol-4-ylboronic acid

https://huagongshe.com/reaction/369037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl borateHCID 9009—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-2,1,3-benzoxadiazoleHCID 607823—
ReactantButyllithiumHCID 178418339—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductB-2,1,3-Benzoxadiazol-4-ylboronic acidHCID 2118680532%

Reaction Steps

To a solution of 4-benzo[c]furazanyl bromide (4 g, 0.020 mol) in tetrahydrofurane (80 ml) and n-pentane (20 ml) is added triethylborate (3.8 ml, 0.022 mol) and N,N,N,N-tetraethylendiamine (3 ml, 0.02 mol). Then, n-BuLi (8.8 ml, 2.5N in hexane, 0.022 mol) is added dropwise at -100° C. and the solution is stirred for 5 minutes more. The reaction mixture is poured into an aqueous solution of saturated ammonium chloride and the water phase is extracted with ethyl acetate. The organic solvent is removed and the crude product is taken up in dichloromethan/n-hexane (5:6). The suspension is filtered to yield the title compound (1.05 g) which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136821
Source datasetuspto-grants-2000_10
ORD IDord-4ebbced45bb6440c905812d638390ec3
Source noteuspto-grants-2000_10