HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55276Generated: October 27, 2026
Water → (6-Iodo-5-methoxypyridin-2-yl)methanol
https://huagongshe.com/reaction/55276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 6-iodo-5-methoxypicolinate | HCID 49766559 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Iodo-5-methoxypyridin-2-yl)methanol | HCID 19957482 | 103.3% |
Reaction Steps
40 ml of a 25% solution of diisobutylaluminum hydride in toluene is added drop by drop to a solution of 7 g of 2-iodo-3-methoxypyridine-6-carboxylic acid methyl ester in 95 ml of toluene and 50 ml of tetrahydrofuran at -70° C. The reaction mixture is stirred for 30 minutes at -70° C., heated to -5° C. within two hours and stirred for 2 hours at this temperature. The reaction mixture is cooled to -70° C., mixed in succession with 20 ml of isopropanol and 20 ml of water and stirred for three hours at room temperature. The precipitate is suctioned off on diatomaceous earth, the filter residue is washed with dichloromethane and the filtrate is concentrated by evaporation. 6.54 g of 6-hydroxymethyl-2-iodo-3-methoxypyridine of melting point 106°-108° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624943 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-30ed483f116d457da5fce53a19b52087 |
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| Source note | uspto-grants-1997_04 |
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