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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037027Generated: November 1, 2026

Triisopropyl borate → 3,3-bis(fluoromethyl)-6-methylbenzo[c][1,2]oxaborol-1(3H)-ol

https://huagongshe.com/reaction/1037027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant2-Bromo-1-(1,3-difluoro-2-(methoxymethoxy)propan-2-yl)-4-methylbenzeneHCID 86685473—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3,3-bis(fluoromethyl)-6-methylbenzo[c][1,2]oxaborol-1(3H)-olHCID 8668547260.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-bromo-1-(1,3-difluoro-2-(methoxymethoxy)propan-2-yl)-4-methylbenzene (1.2 g, 3.9 mmol) in THF (20 mL) at −78° C. was added n-BuLi (4 mL, 9.75 mmol) dropwise. The mixture was stirred at −78° C. for additional 1 h and then triisopropyl borate (1.5 g, 7.9 mmol) in 10 mL of THF was added below −70° C. The resulting mixture was kept stirring at −78° C. for 30 min and allowed to warm to rt and stirred overnight. Then it was quenched with aqueous NH4Cl and extracted with EA. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The residue was purified on column chromatography to provide the product (0.5 g, yield 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546357B2
Source datasetuspto-grants-2013_10
ORD IDord-b1ff79f610cb4007879e2b3ab5fb9230
Source noteuspto-grants-2013_10