HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248280Generated: October 30, 2026
Trifluoromethanesulfonic acid → HCID 57154952, compound
https://huagongshe.com/reaction/248280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Allyl 2,2,2-Trichloroacetimidate | HCID 316905 | — |
| Reactant | 17-Ethyl-1-hydroxy-12-[2'-(4"(tert-butyldimethylsiloxy)-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 | HCID 57014474 | — |
| Product | HCID 57154952 | HCID 57154952 | — |
Reaction Steps
To a solution of 17-ethyl-1-hydroxy-12-[2'-(4"(tert-butyldimethylsiloxy)-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 (186 mg in 6 ml 33% methylene chloride in cyclohexane) allyltrichloroacetimidate (62 μl neat) was added and the reagents allowed to mix for 5 minutes. Trifluoromethanesulfonic acid (5 μl neat) was added slowly via syringe and the mixture stirred at room temperature. After 24 hours the reaction was quenched by the addition of saturated sodium bicarbonate and extracted with ethyl acetate (3×5 ml). The combined organics were washed with brine and dried over magnesium sulfate. Purification of the concentrate by flash chromatography on silica gel (ethyl acetate: hexane (1:4)+1% methanol) gave the title compound (80 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05208228 |
|---|
| Source dataset | uspto-grants-1993_05 |
|---|
| ORD ID | ord-6db4641503d741b8b898328afde1dccb |
|---|
| Source note | uspto-grants-1993_05 |
|---|