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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423209Generated: October 30, 2026

Tributylphosphine → 3-Bromo-2-(5-chloro-2-iodo-phenoxymethyl)-pyridine

https://huagongshe.com/reaction/423209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant5-Chloro-2-iodophenolHCID 6613333—
Reactant(3-Bromopyridin-2-yl)methanolHCID 14022521—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-2-(5-chloro-2-iodo-phenoxymethyl)-pyridineHCID 5924295151%

Reaction Conditions

Temperature0 °C

Reaction Steps

(3-Bromo-pyridin-2-yl)-methanol (3.4 g, 18 mmol), and 2-iodo-5-chlorophenol 4.5 g, 18 mmol), are dissolved in benzene (60 mL) and cooled to 0° C. To the solution is added tributylphosphine (15 mL, 90 mmol), and 1,1′-(azodicarbonyl) dipiperidine (ADDP) (6.6 g, 18 mmol) and the mixture is heated at 40° C. for 3 h. The reaction mixture is diluted with ethyl acetate, washed with saturated aqueous NH4Cl and brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (Biotage® Si65M, 15% ethyl acetate/hexane) to yield 3.77 g (51%) of the title compound as a white solid. GCMS m/e 296, 298 [M-I]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101760B2
Source datasetuspto-grants-2012_01
ORD IDord-3abff213d76c4d6198aae4913573ee7d
Source noteuspto-grants-2012_01