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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459105Generated: October 30, 2026

Trifluoromethanesulfonate → HCID 58822907, compound

https://huagongshe.com/reaction/459105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonateHCID 2758875—
ReactantHCID 18443698HCID 18443698—
ReactantHCID 58822780HCID 58822780—
ProductHCID 58822907HCID 58822907—

Reaction Steps

The title compound was prepared from 6-But-3-ynyloxy-3-(4-fluoro-phenyl)-benzofuran and (2S)-2-methoxy-3-(4-trifluoromethanesulfonyloxy-phenyl)-propionic acid ethyl ester Example 1, Step A) following the procedure described in Example 40, Step C. The ethyl ester derivative was contaminated with starting triflate. The mixture was hydrolyzed using the Standard Procedure C. The residue was purified by chromatography. MS(ES) for C28H23FO5 [M−H]−: 457.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192982B2
Source datasetuspto-grants-2007_03
ORD IDord-f0df2f06000f467fa87dbc496e621e0b
Source noteuspto-grants-2007_03