HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656235Generated: October 29, 2026
Methyl iodide → 5-Bromo-2-methoxy-3-(3-methoxypropoxy)-pyridine
https://huagongshe.com/reaction/656235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 5-bromo-3-(3-methoxypropoxy)-1H-pyridin-2-one | HCID 23149475 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-Bromo-2-methoxy-3-(3-methoxypropoxy)-pyridine | HCID 23149492 | — |
Reaction Steps
A mixture of 113.26 mmol of 5-bromo-3-(3-methoxypropoxy)-1H-pyridin-2-one, 79.28 mmol of silver carbonate and 158.56 mmol of iodomethane in 230 ml of benzene is stirred at 45° C. with exclusion of light for 24 hours. The reaction mixture is cooled to room temperature, and the silver salts are filtered off. The filtrate is washed with 2% sodium bicarbonate solution and water (2×). The organic phase is dried over sodium sulphate and evaporated. The crude title compound is obtained as a beige oil from the residue and is employed without further purification in the next stage. Rf=0.45 (EtOAc-heptane 1:2); Rt=4.34 (Gradient I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071651B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-2458b09a853349989fa62fcf49c6f0e3 |
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| Source note | uspto-grants-2011_12 |
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