HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082632Generated: November 1, 2026
Trifluoromethanesulfonic acid → HCID 86746580, compound
https://huagongshe.com/reaction/2082632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Allyl 2,2,2-Trichloroacetimidate | HCID 316905 | — |
| Reactant | HCID 86746581 | HCID 86746581 | — |
| Solvent | Dichloromethane cyclohexane | HCID 21916607 | — |
| Product | HCID 86746580 | HCID 86746580 | — |
Reaction Steps
To a solution of 17-ethyl-20-fluoro-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 | US05189042 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-9328814c574945268e658a3de5fc19de |
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| Source note | uspto-grants-1993_02 |
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