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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531474Generated: November 1, 2026

Acetic Acid → (5-Bromo-2-fluorophenyl)boronic acid

https://huagongshe.com/reaction/1531474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTrimethyl borateHCID 8470—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantLithium diisopropylamideHCID 2724682—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(5-Bromo-2-fluorophenyl)boronic acidHCID 1085697499%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of lithium diisopropylamide (165 mL of a 2.0 M solution in tetrahydrofuran, 0.33 mol) in tetrahydrofuran (600 mL) at −70° C. is treated with 1-bromo-4-fluorobenzene (33.0 mL, 0.30 mol), stirred at −70° C. for 90 minutes and added to a solution of trimethyl borate (41.0 mL, 0.36 mol) in diethyl ether (300 mL) at −70° C. The resulting solution is stirred at −70° C. for 15 minutes, warmed to 15° C. over 90 minutes, treated with acetic acid (51.5 mL, 0.9 mol) and water (375 mL), and stirred at room temperature for 30 minutes. The organic layer is separated and the aqueous layer is extracted with ether. The organic extracts are combined with the organic layer and the resulting solution is washed sequentially with 10% hydrochloric acid and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to give the title product as an off-white solid (65 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06198008B1
Source datasetuspto-grants-2001_03
ORD IDord-129df2ea92bf42cfb05dfc459d1519e6
Source noteuspto-grants-2001_03