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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082632Generated: November 1, 2026

Trifluoromethanesulfonic acid → HCID 86746580, compound

https://huagongshe.com/reaction/2082632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantAllyl 2,2,2-TrichloroacetimidateHCID 316905—
ReactantHCID 86746581HCID 86746581—
SolventDichloromethane cyclohexaneHCID 21916607—
ProductHCID 86746580HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189042
Source datasetuspto-grants-1993_02
ORD IDord-9328814c574945268e658a3de5fc19de
Source noteuspto-grants-1993_02