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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767621Generated: October 30, 2026

Hydrochloric Acid → 2-Methoxy-5-(trifluoromethyl)phenylboronic acid

https://huagongshe.com/reaction/1767621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant1-Methoxy-4-(trifluoromethyl)benzeneHCID 600604—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-5-(trifluoromethyl)phenylboronic acidHCID 278267681.8%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 4-trifluoromethylanisole (8 g; 45 mmol) in dry THF (80 ml) at −30° C. under N2 was added a solution of 2.5 M n-BuLi in hexane (20 ml; 50 mmol). The reaction mixture was stirred for 1 h at −30° C., then cooled to −70° C. and added B(Oi-Pr)3 (14.1 ml; 64 mmol). The reaction mixture was allowed to slowly warm up to rt. over night. The reaction mixture was added 2 M HCl (40 ml) and THF was removed by evaporation. The aqueous remanense was extracted with Et2O (4×20 ml) and the combined organic fractions were extracted with 1 M NaOH (5×17 ml). The combined aqueous fractions were neutralized by 10 M HCl. The precipitate formed was isolated by filtration and washed with 1 M HCl to give 8.1 g (81%) product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235548B2
Source datasetuspto-grants-2007_06
ORD IDord-67183aac018141ab8ad6c4784413459a
Source noteuspto-grants-2007_06