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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496791Generated: October 29, 2026

Hydrochloric Acid → (2-Ethylthiophenyl)boronic acid

https://huagongshe.com/reaction/496791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant1-Bromo-2-(ethylsulfanyl)benzeneHCID 13082725—
ReactantButyllithiumHCID 178418339—
SolventEthyl AcetateHCID 8857—
Product(2-Ethylthiophenyl)boronic acidHCID 3785655—

Reaction Conditions

Temperature-70 °C

Reaction Steps

9.5 g (50 mmol) of triisopropyl borate are added to a solution of 10.9 g (50.0 mmol) of 1-bromo-2-ethylsulfanylbenzene kept at −70° C. 33.3 ml of a 15% solution of BuLi in hexane (55 mmol) are then added. The mixture is stirred at −70° C. for a further 30 minutes, then 1 N hydrochloric acid and ethyl acetate are added. The organic phase is separated off, dried and evaporated. The residue is taken up in diethyl ether and filtered. A colourless solid is obtained; FAB 182

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946489B2
Source datasetuspto-grants-2005_09
ORD IDord-8215473de7e84f9db4a581d52f40e108
Source noteuspto-grants-2005_09