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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198056Generated: October 25, 2026

Hydrochloric Acid → [2-Methoxy-3-(trifluoromethyl)phenyl]boronic acid

https://huagongshe.com/reaction/2198056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant1-Methoxy-2-(trifluoromethyl)benzeneHCID 2775251—
ReactantHCID 67022311HCID 67022311—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product[2-Methoxy-3-(trifluoromethyl)phenyl]boronic acidHCID 4535843083%

Reaction Steps

To a solution of 1-methoxy-2-(trifluoromethyl)benzene (6.30 g, 35.8 mmol) in THF (150 mL) was added n-BuLi (21.0 ml, 2.50 M hexane solution, 53.7 mmol), and the mixture was stirred at room temperature for 1 hr. The solution was cooled to −78° C., tris(1-methylethyl)borate (8.08 g, 43.0 mmol) was added, and the mixture was stirred at −78° C. for 0.5 hr. The reaction solution was allowed to cool to room temperature and stirred for 16 hr. The mixture was acidified with 1M hydrochloric acid and extracted with ethyl acetate (300 mL). The extract was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give a mixture (6.52 g, yield 83%) of [2-methoxy-3-(trifluoromethyl)phenyl]boronic acid and [3-methoxy-2-(trifluoromethyl)phenyl]boronic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338622B2
Source datasetuspto-grants-2012_12
ORD IDord-694e63a1b94743f18cb1119bbb1180c5
Source noteuspto-grants-2012_12