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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024923Generated: October 25, 2026

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

https://huagongshe.com/reaction/1024923

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 numberUS08722883B2
Source datasetuspto-grants-2014_05
ORD IDord-75a2dfb8b1ca4cf6b58a32ea19798a9d
Source noteuspto-grants-2014_05