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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274585Generated: October 25, 2026

Acetic Acid → Ethyl 5-amino-1,2-benzisothiazole-3-acetate

https://huagongshe.com/reaction/1274585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDichloromethaneHCID 6344—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 5-nitro-1,2-benzisothiazole-3-acetateHCID 18314495—
CatalystIronHCID 23925—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-amino-1,2-benzisothiazole-3-acetateHCID 11770464—

Reaction Conditions

Temperature50 °C

Reaction Steps

A 10% acetic acid solution (31.0 mL) is stirred at 50° C., treated with iron powder (0.656 g), treated dropwise with a solution of ethyl 5-nitro-1,2-benzisothiazole-3-acetate (1.03 g, 3.88 mmol) in ethyl acetate, stirred at 50° C. for two hours, treated with additional iron powder (0.305 g), stirred at 50° C. for 15 minutes, and poured into saturated sodium hydrogen carbonate solution. The resultant aqueous mixture is extracted with ethyl acetate. The combined organic extracts are washed sequentially with water and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo to obtain an oil. Column chromatography of the oil using silica gel and methylene chloride gives the title product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156700
Source datasetuspto-grants-2000_12
ORD IDord-8c5e340803814942b4a92a6bc4f8c31a
Source noteuspto-grants-2000_12