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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003701Generated: October 30, 2026

Trifluoromethanesulfonic anhydride → HCID 22132527, compound

https://huagongshe.com/reaction/1003701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 22132507HCID 22132507—
CatalystCopper SulfateHCID 24462—
SolventPyridineHCID 1049—
ProductHCID 22132527HCID 2213252733%

Reaction Steps

Trifluoromethanesulfonic anhydride (0.53 ml, 3.14 mmol) was added dropwise with stirring to an ice-cooled solution of 7-hydroxy-2-(4-phthalimidobutyl)-1,2,3,4-tetrahydroisoquinoline (1 g, 2.86 mmol) in anhydrous pyridine (10 ml). After stirring at room temperature for 18 h the reaction mixture was added to 10% aqueous Copper (II) sulfate (100 ml) and extracted into ethyl acetate (200 ml). The organic layer was separated, washed with 10% aqueous copper (II) sulfate (2×50 ml), dried (Na2SO4) and evaporated in vacuo. Chromatography on silica gel using 10-100% ethyl acetate-hexane gradient elution gave the title compound as a green oil (0.45 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046210
Source datasetuspto-grants-2000_04
ORD IDord-3031a190d741444d9eea75e0ed53c366
Source noteuspto-grants-2000_04