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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | 5-Chloro-2-iodophenol | HCID 6613333 | — |
| Reactant | (3-Bromopyridin-2-yl)methanol | HCID 14022521 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Bromo-2-(5-chloro-2-iodo-phenoxymethyl)-pyridine | HCID 59242951 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101760B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-3abff213d76c4d6198aae4913573ee7d |
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| Source note | uspto-grants-2012_01 |
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