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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388800Generated: November 2, 2026

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

https://huagongshe.com/reaction/2388800

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 numberUS08269002B2
Source datasetuspto-grants-2012_09
ORD IDord-fc759bd5c12147cd8fe38e5e1832e6b1
Source noteuspto-grants-2012_09