HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854206Generated: November 1, 2026
HCID 58932261, compound → HCID 58932232, compound
https://huagongshe.com/reaction/854206
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58932261 | HCID 58932261 | — |
| Reactant | HCID 86601416 | HCID 86601416 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58932232 | HCID 58932232 | 93.4% |
Reaction Steps
A 0.2M guanidine/guanidine nitrate solution (methanol-methylene chloride, 9:1)(3.9 mL, 0.78 mmol) was added to (8E,12E,14E)-7-acetoxy-3,21-bis(diethylisopropylsiloxy)-16-hydroxy-6,10,12,16,20-pentamethyl-18,19-epoxytricosa-8,12,14-trien-11-olide (307 mg, 0.3868 mmol), and the reaction mixture was stirred at room temperature for 13 hours. The reaction mixture was diluted with ethyl acetate, and then the organic layer was washed with an aqueous solution of ammonium chloride. The resulting organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (Kanto silica gel 60N, 40 to 50 μm; ethyl acetate-hexane, 1:4) to obtain the title compound (271.5 mg, 93%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256178B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-c7b4c70024554dab95cfa7da8d9a8ba3 |
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| Source note | uspto-grants-2007_08 |
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