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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369603Generated: October 25, 2026

Hydrochloric Acid → Ethyl alpha-cyano-5-nitro-1,2-benziso-thiazole-3-acetate

https://huagongshe.com/reaction/369603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl cyanoacetateHCID 7764—
Reactant1,2-Benzisothiazole, 3-chloro-5-nitro-HCID 198098—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductEthyl alpha-cyano-5-nitro-1,2-benziso-thiazole-3-acetateHCID 12607115—

Reaction Steps

A sodium ethoxide solution (previously prepared from ethanol and sodium (1.00 g, 0.0430 mol)) is cooled with an ice-acetone bath, treated portionwise with ethyl cyanoacetate (4.51 g, 0.0398 mol), stirred at room temperature for 30 minutes, treated with 3-chloro-5-nitro-1,2-benzisothiazole (4.27 g, 0.0199 mol), stirred at room temperature overnight, cooled to 0° C., and treated dropwise with 10% hydrochloric acid (15.0 mL). The resultant aqueous mixture is stirred at room temperature for one hour and filtered to obtain a solid. The solid is washed with ethanol and air-dried to give the title product as a yellow solid which is identified by NMR spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140270
Source datasetuspto-grants-2000_10
ORD IDord-2b7f1acdbdb54381ab732e54979003eb
Source noteuspto-grants-2000_10