HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877089Generated: November 1, 2026
Water → 5-{4-[Chloro(cyclohexyl)methyl]-5-(methoxymethyl)furan-2-yl}-2-methoxypyridine
https://huagongshe.com/reaction/1877089
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Cyclohexyl[2-(methoxymethyl)-5-(6-methoxypyridin-3-yl)furan-3-yl]methanol | HCID 68514162 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-{4-[Chloro(cyclohexyl)methyl]-5-(methoxymethyl)furan-2-yl}-2-methoxypyridine | HCID 68512488 | 100% |
Reaction Steps
To a solution of cyclohexyl[2-(methoxymethyl)-5-(6-methoxypyridin-3-yl)furan-3-yl]methanol (0.8 g) in toluene (10 mL) were added thionyl chloride (0.2 mL) and pyridine (0.3 mL) at 0° C., and the mixture was stirred at 0° C. for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (0.8 g, 100%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309580B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-66fd55bace88448cb250955a264a36b2 |
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| Source note | uspto-grants-2012_11 |
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