Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514006Generated: November 3, 2026

Hexane → (6-Phenylnaphthalen-2-yl)boronic acid

https://huagongshe.com/reaction/1514006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant2-Bromo-6-phenylnaphthaleneHCID 15311215—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product(6-Phenylnaphthalen-2-yl)boronic acidHCID 5753961387.6%

Reaction Conditions

Temperature-10 °C

Reaction Steps

In an atmosphere of argon, 360 g (1.27 mol) of 2-bromo-6-phenylnaphthalene, 2 L of dehydrated diethyl ether and 2 L of dehydrated toluene were charged and cooled to −10° C. Then, 1 L (1.58 mol) of a hexane solution of 1.58M n-butyl lithium was added dropwise, and stirred at −10° C. for 5 hours. The reaction solution was cooled to −60° C., and after adding 718 g (3.81 mol) of triisopropyl borate, the mixture was stirred at room temperature for 17 hours. After adding 1 L of toluene and 1 L of water, the resulting mixture was stirred for an hour. Then, an aqueous layer was removed. An organic layer was washed with water, and dried with magnesium sulfate. The organic layer was concentrated, and heat-washed with toluene, whereby 276 g of 6-phenylnaphthalene-2-boronic acid was obtained (yield: 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08221907B2
Source datasetuspto-grants-2012_07
ORD IDord-2549a37f851d4cf98f5c8c97e59222d7
Source noteuspto-grants-2012_07