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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277388Generated: October 30, 2026

Acetic Acid → [(5-Amino-1,2-benzisothiazol-3-yl)oxy]acetonitrile

https://huagongshe.com/reaction/277388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant[(5-Nitro-1,2-benzisothiazol-3-yl)oxy]acetonitrileHCID 18314467—
CatalystIronHCID 23925—
SolventEthyl AcetateHCID 8857—
Product[(5-Amino-1,2-benzisothiazol-3-yl)oxy]acetonitrileHCID 18314508—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of iron powder (13.0 g, 0.233 mol) in a 5% acetic acid solution (65.0 mL) is heated to 50° C., treated portionwise with a mixture of [(5-nitro-1,2-benzisothiazol-3-yl)oxy]acetonitrile (11.0 g, 0.047 mol), acetic acid (100 mL) and ethyl acetate (65.0 mL), refluxed for two hours, cooled to 40° C., and filtered to remove solids. The phases are separated and the aqueous phase is extracted with ethyl acetate. The organic phase and the organic extracts are combined, washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to give the title product as an oil which is identified by NMR spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355796B1
Source datasetuspto-grants-2002_03
ORD IDord-062235424fb04485a7ba3c8cef232ed4
Source noteuspto-grants-2002_03