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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175428Generated: October 25, 2026

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

https://huagongshe.com/reaction/1175428

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 (300 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 numberUS07838675B2
Source datasetuspto-grants-2010_11
ORD IDord-9977a721b955460186cc2ba04c48489f
Source noteuspto-grants-2010_11