HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980071Generated: October 29, 2026
2,4,6-Trimethylpyridine → HCID 13826528, compound
https://huagongshe.com/reaction/980071
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | HCID 13826525 | HCID 13826525 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 13826528 | HCID 13826528 | — |
Reaction Steps
A mixture of 0.605 g. (0.0010 mole) of [1α,3β,7ξ,24R]-7-bromo-24-fluorocholest-5-en-1,3,25-triol 1,3-diacetate, 0.6 ml. of s-collidine and 18 ml. of xylene was heated at reflux (140° C.) for 0.5 hr and cooled. The mixture was diluted with 30 ml. of toluene This solution was washed with 10% aqueous sulfuric acid, and saturated aqueous sodium bicarbonate solution. The organic phase was dried over anhydrous magnesium sulfate, filtered, and evaporated to dryness. The residue was purified by column chromatography on 0.06-0.20 mm silica gel to yield [1α,3β,24R]-24-fluorocholesta-5,7-dien-1,3,25-triol 1,3-diacetate, [α]D23 -21° (c 0.5, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04634692 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-a4d3a286a041462ea4f86209a7dd71be |
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| Source note | uspto-grants-1987_01 |
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