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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384006Generated: October 30, 2026

Hydrochloric Acid → 3-Isopropylbenzeneboronic acid

https://huagongshe.com/reaction/2384006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant1-Bromo-3-isopropylbenzeneHCID 138499—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Isopropylbenzeneboronic acidHCID 277347893.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-BuLi (7.7 mL, 14.0 mmol) was added dropwise to a stirred solution of 1-bromo-3-isopropyl-benzene (2.4 g, 12.1 mmol) in dry THF (40 mL) over 30 min at −70° C. under nitrogen. The reaction mixture was degassed for 15 min, and triisopropylborate (2.63 g, 14.0 mmol) was added at the same temperature. The reaction mixture was gradually warmed to 0° C. during 90 min and stirred for an additional 30 min at 0° C. The reaction mixture was then cooled to −20° C., and an aqueous solution of 2N HCl (20 mL) was added slowly. THF was distilled off and the reaction mixture was extracted with ethyl acetate (2×20 mL). The combined organic layers were dried over Na2SO4, and concentrated in vacuo to obtain the crude product (1.85 g, 93.5%), which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263656B2
Source datasetuspto-grants-2012_09
ORD IDord-fd1ff9c0ecbd4f2ea6b64bbf3f5318db
Source noteuspto-grants-2012_09