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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216713Generated: October 26, 2026

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → 1-Methyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine

https://huagongshe.com/reaction/216713

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
Reactant1-(4-Bromophenyl)-4-methylpiperazineHCID 11817675—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
Product1-Methyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazineHCID 17998905—

Reaction Steps

To a cooled (−78° C.) solution of 1-(4-Bromo-phenyl)-4-methyl-piperazine (8.05 g, 31.54 mmol, CAS 130307-08-3) in dry THF (500 ml) are added dropwise 28 ml of a solution of n-BuLi (2.5M in hexanes, 69 mmol). After 1 h, of 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (13.1 ml, 63.1 mmol) in solution in dry THF (20 ml) are introduced. After complete addition, the reaction mixture is allowed to slowly warm up to RT. The reaction mixture is then diluted with 200 ml of a saturated solution of NH4Cl and most of the THF is removed by evaporation. The residue is diluted with EtOAc and the phases are separated. The aqueous phase is re-extracted three times with EtOAc and the combined organic extracts are washed twice with de-ionized water, once with saturated brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue is purified by chromatography (silicagel, CH2Cl2/EtOH 9:1) to afford the title compound as a colorless solid, Rt=0.851 min (Acquity HPLC BEH C18, 2.1×50 mm, 1.7 micron, detection 215 nM, 0.1 min 2% CH3CN in H2O, 2% to 100% CH3CN in H2O in 1.5 min, 0.4 min 100% CH3CN+0.1% TFA, flow rate 1.0 ml/min); MS: 303 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193189B2
Source datasetuspto-grants-2012_06
ORD IDord-35d49eea4f44401390691136571ed0e3
Source noteuspto-grants-2012_06