Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19829Generated: October 24, 2026

Hydrochloric Acid → 4-Cyclopropylbenzeneboronic acid

https://huagongshe.com/en/reaction/19829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant1-Bromo-4-cyclopropylbenzeneHCID 12221355—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Cyclopropylbenzeneboronic acidHCID 2849428—

Reaction Conditions

Temperature-70 °C

Reaction Steps

2.5 M nButyllithium in hexane (14.5 mL) is added dropwise to 1-bromo-4-cyclopropyl-benzene (5.92 g) in THF (14 mL) and toluene (50 mL) chilled to −70° C. The resultant solution is stirred at −70° C. for 30 min before triisopropyl borate (8.5 mL) is added. The solution is warmed to −20° C. and then treated with 4 M aqueous hydrochloric acid (15.5 mL). The reaction mixture is further warmed to room temperature and then the organic phase is separated. The aqueous phase is extracted with ethyl acetate and the combined organic phases are dried (sodium sulphate). The solvent is evaporated and the residue is washed with a mixture of ether and cyclohexane to give the product as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745414B2
Source datasetuspto-grants-2010_06
ORD IDord-0ba6ce0f6e0e40739ff825ced6ba4d1c
Source noteuspto-grants-2010_06