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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452640Generated: October 30, 2026

Hydrochloric Acid → 4-(Methylsulfanyl)-3-(trifluoromethoxy)phenylboronic acid

https://huagongshe.com/reaction/452640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant4-Bromo-2-(trifluoromethoxy)thioanisoleHCID 18711473—
SolventTetrahydrofuranHCID 8028—
Product4-(Methylsulfanyl)-3-(trifluoromethoxy)phenylboronic acidHCID 6866438571%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-bromo-1-(methylthio)-2-(trifluoromethoxy)benzene (6.63 g, 23.1 mmol) and triisopropyl borate (6.92 mL, 30.0 mmol) in tetrahydrofuran (50 mL) was added dropwise 1.6 M n-butyllithium-hexane solution (25.0 mL, 40.0 mmol) at −78° C., and the resulting mixture was stirred for 30 min. The reaction mixture was warmed to 0° C., 2 M hydrochloric acid (150 mL) was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was washed with hexane/ethyl acetate (5/1) and recrystallized from hexane/tetrahydrofuran to give the title compound (4.13 g, yield 71%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-5d5db01571214d079710b5ed90f2b57c
Source noteuspto-grants-2013_07