HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734366Generated: October 29, 2026
Pyridine, hydrofluoride (1:1) → HCID 57075111, compound
https://huagongshe.com/reaction/1734366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine, hydrofluoride (1:1) | HCID 64774 | — |
| Reactant | HCID 57054354 | HCID 57054354 | — |
| Reactant | HCID 178435178 | HCID 178435178 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57075111 | HCID 57075111 | — |
Reaction Steps
To a solution of 17-ethyl-1,14-dihydroxy-12-[2'-(4"-(4'"-t-butyldimethylsiloxycinnamyloxy)-3"-methoxycyclohexyl)-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone (190 mg in 2 ml tetrahydrofuran contained in a polypropylene vial) was added 500 μl of a solution of hydrogen fluoride-pyridine complex (40% in (2:1) tetrahydrofuran:pyridine) and the mixture stirred at room temperature. After 2 hours, the reaction was quenched by the careful addition of saturated sodium bicarbonate and extracted with ethyl acetate. The combined organics were dried over magnesium sulfate, concentrated in vacuo and purified by flash chromatography on silica gel (ethyl acetate:hexane (2:1) to give the title compound (50 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05532248 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-3aa3049c2715495789af0566370652ed |
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| Source note | uspto-grants-1996_07 |
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