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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971092Generated: October 26, 2026

Phosphoric Acid → (3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acid

https://huagongshe.com/reaction/971092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantTriisopropyl borateHCID 21531—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-(3-bromophenyl)piperazine-1-carboxylateHCID 10882380—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventHeptaneHCID 8900—
SolventTetrahydrofuran tolueneHCID 22635083—
Product(3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acidHCID 22392008—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To the 4-tert-Butyloxycarbonyl-1-(3-bromophenyl)piperazine from Step 1 (118.30 g, 346.9 mmol) in tetrahydrofuran/toluene (1/1, 1.5 L) at −78° C. under nitrogen was added n-butyllithium (2.5M, 160 mL, 398.9 mmol) dropwise and the resulting reaction mixture was stirred at −78° C. for 20 minutes. Triisopropyl borate (96.4 mL, 416.3 mmol) was added dropwise and the reaction was warmed to 0° C. and stirred for 2 hours. Aqueous saturated ammonium chloride (400 mL), water (100 mL) and 1 equivalent of H3PO4 (20 mL) were added and the mixture was stirred for 15 minutes and then concentrated to a volume of approximately 200 mL (at which stage the mixture became bluish and a precipitate formed). The mixture was slowly diluted with heptane (800 mL) and the resulting suspension was stirred overnight. The suspension was filtered, the solid was washed with heptane and dried to afford the title boronic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312334B2
Source datasetuspto-grants-2007_12
ORD IDord-841f4d3d7ddc4b06a2cb958094345a70
Source noteuspto-grants-2007_12