Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954182Generated: November 1, 2026

Triisopropyl borate → 3-Benzyloxy-phenylboronic acid

https://huagongshe.com/reaction/1954182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Benzyloxy-phenylboronic acidHCID 2734313—

Reaction Steps

A solution of 3-benzyloxy-bromobenzene 10 g (38 mmol) in 150 mL of anhydrous THF was cooled to -70° C. under a nitrogen atmosphere. 28.5 mL of n-butyl lithium (1.6 M in hexanes) was added dropwise to the solution. The reaction mixture was stirred for 30 minutes, then tri-isopropyl borate 10.6 mL (45.6 mmol) was added. The reaction mixture was allowed to warm to ambient temperature over a two hour period. The reaction was quenched by the addition of 200 mL of 1 N HCl and the reaction mixture was stirred for an additional hour. The slurry was extracted twice with EtOAc and the organic layer separated and combined. The EtOAc solution was washed twice with brine, dried with Na2SO4, and evaporated to a yellow oil. The product was crystallized from ether-hexane. This yielded 4.85 g of the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06121293
Source datasetuspto-grants-2000_09
ORD IDord-e85cfaec59a74c76a1b17867a3633f1a
Source noteuspto-grants-2000_09