HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865593Generated: October 31, 2026
Trifluoromethanesulfonic acid → HCID 86747275, compound
https://huagongshe.com/reaction/865593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Allyl 2,2,2-Trichloroacetimidate | HCID 316905 | — |
| Reactant | HCID 57019030 | HCID 57019030 | — |
| Solvent | Dichloromethane cyclohexane | HCID 21916607 | — |
| Product | HCID 86747275 | HCID 86747275 | — |
Reaction Steps
To a solution of 17-ethyl-1,14-dihydroxy-12-[2'-(4"-(napth-2-yloxy)-3"-hydroxycyclohexyl)-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 in 33% methylene chloride/cyclohexane is added 1.5 equivalents of allyl trichloroacetimidate, and the reagents are allowed to mix for 5 minutes. A catalytic amount of trifluoromethanesulfonic acid is then added slowly via syringe and the mixture is stirred at room temperature. After 3 hours the reaction is quenched by the addition of saturated sodium bicarbonate and extracted with ethyl acetate. The combined organics are washed with brine and dried over magnesium sulfate. Purification of the concentrate by flash chromatography on silica gel gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05565560 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-1b6f418ceaa64dddb91aefce319ec4f8 |
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| Source note | uspto-grants-1996_10 |
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