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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780295Generated: November 1, 2026

3-Nitrophenylboronic Acid → HCID 9843146, compound

https://huagongshe.com/reaction/1780295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
ReactantSodium CarbonateHCID 10340—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-5-((S)-1-methyl-pyrrolidin-2-ylmethoxy)-pyridineHCID 11288721—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 9843146HCID 984314660%

Reaction Steps

To a solution of 5-bromo-3-((1-methyl-2-(S)-pyrrolidinyl)methoxy)pyridine (272 mg, 1.00 mmol) in benzene (2.0 mL), were added sodium carbonate (2.0M, 1.0 mL), tetrakis(triphenylphosphine)palladium(0) (35 mg, 0.03 mmol) and 3-nitrophenylboronic acid (250 mg, 1.50 mmol). The reaction mixture was refluxed overnight then cooled to room temperature. Water (2 mL) was added, and solid sodium bicarbonate was added until the aqueous layer was saturated. The mixture was extracted with EtOAc, which was dried over MgSO4, filtered and concentrated. The residue was chromatographed on a silica gel column, eluting with NH4OH/MeOH/EtOAc 0:1:9 and 1:10:90 to afford a light yellowish oil (187 mg, 60%). MS (CI/NH3) m/z 314 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ1.72-1.97 (m, 3H), 2.03-2.14 (m, 1H), 2.30-2.47 (m, 1H), 2.53 (s, 3H), 2.67-2.80 (m, 1H), 3.12-3.22 (m, 1H), 4.00-4.15 (m, 2H), 7.43-7.46 (m, 1H), 7.63-7.70 (m, 1H), 7.88-7.94 (m, 1H), 8.25-8.31 (m, 1H), 8.38-8.51 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629325
Source datasetuspto-grants-1997_05
ORD IDord-16a4e651aa774906a45553e1d5e0e936
Source noteuspto-grants-1997_05