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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655799Generated: October 31, 2026

Trifluoromethanesulfonic acid → HCID 86747275, compound

https://huagongshe.com/reaction/1655799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantAllyl 2,2,2-TrichloroacetimidateHCID 316905—
ReactantHCID 57019030HCID 57019030—
SolventDichloromethane cyclohexaneHCID 21916607—
ProductHCID 86747275HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250678
Source datasetuspto-grants-1993_10
ORD IDord-00c2b162118a4872b1029107d21ed45f
Source noteuspto-grants-1993_10