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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596413Generated: October 29, 2026

Sulfuric Acid → 4,4,5,5-Tetramethyl-2-[3-(trifluoromethoxy)phenyl]-1,3,2-dioxaborolane

https://huagongshe.com/reaction/1596413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPinacolHCID 6425—
ReactantTrimethyl borateHCID 8470—
Reactant1-Bromo-3-(trifluoromethoxy)benzeneHCID 519964—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product4,4,5,5-Tetramethyl-2-[3-(trifluoromethoxy)phenyl]-1,3,2-dioxaborolaneHCID 2760602—

Reaction Steps

2.41 g of 3-(trifluoromethoxy)brombenzene are dissolved in 25 ml of diethyl ether and added dropwise to a suspension of 0.28 g of magnesium in 25 ml of diethyl ether such that the solution remains at the boil. After addition is complete, the mixture is stirred under reflux for 2 h. The cooled solution is added dropwise to a solution of 1.16 ml of trimethyl borate in 25 ml of diethyl ether at a temperature of <−50° C. and then stirred at room temperature for 2 h. 5 ml of 40% strength sulfuric acid and 1.21 g of pinacol are successively added to this solution. After 30 minutes, the solvent is removed on a Rotavapor, the residue is neutralized using saturated sodium hydrogencarbonate solution and the mixture is extracted three times with methyl tert-butyl ether. The organic phase is dried over magnesium sulfate and concentrated in vacuo. 4,4,5,5-Tetramethyl-2-(3-trifluoromethoxyphenyl)-[1,3,2]dioxaborolane is obtained, which is reacted further without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291486B1
Source datasetuspto-grants-2001_09
ORD IDord-f6f11472126748e891f9ed1d3804c11e
Source noteuspto-grants-2001_09