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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284467Generated: October 31, 2026

Hydrochloric Acid → 4-Cyclopropylbenzeneboronic acid

https://huagongshe.com/reaction/2284467

Reaction equation

Participants

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

Reaction Conditions

Temperature-20 °C

Reaction Steps

2.5 M solution of nButyllithium in hexane (14.5 mL) is added dropwise to 1-bromo-4-cyclopropyl-benzene (5.92 g) dissolved in THF (14 mL) and toluene (50 mL) and 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 sulfate). 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 numberUS09145434B2
Source datasetuspto-grants-2015_09
ORD IDord-8569aed9cb53473fac9aaf663837f8a4
Source noteuspto-grants-2015_09