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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958979Generated: October 26, 2026

N-(tert-butyl)-5-cyanofuran-2-sulfonamide → 5-Cyanofuran-2-sulfonamide

https://huagongshe.com/reaction/1958979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-butyl)-5-cyanofuran-2-sulfonamideHCID 53628367—
SolventTrifluoroacetic acidHCID 6422—
Product5-Cyanofuran-2-sulfonamideHCID 53628369—

Reaction Steps

A solution of N-(tert-butyl)-5-cyanofuran-2-sulfonamide (the product of example 50, step i) (1.0 g) in trifluoroacetic acid (30 mL) was stirred at room temperature for 24 h. The mixture was evaporated to dryness in vacuo to leave a crude yellow oil that was triturated with Et2O and filtered. The filtrate was evaporated to dryness in vacuo to give the subtitle compound as a pale yellow oil. Yield: 0.29 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410123B2
Source datasetuspto-grants-2013_04
ORD IDord-894719ac065240739e6c5ce47c677327
Source noteuspto-grants-2013_04