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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369604Generated: October 24, 2026

Acetyl chloride → Ethyl 5-nitro-1,2-benzisothiazole-3-acetate

https://huagongshe.com/en/reaction/369604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantEthyl alpha-cyano-5-nitro-1,2-benziso-thiazole-3-acetateHCID 12607115—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductEthyl 5-nitro-1,2-benzisothiazole-3-acetateHCID 1831449517.1%

Reaction Steps

Ethyl α-cyano-5-nitro-1,2-benzisothiazole-3-acetate (6.67 g, 0.0229 mol) is added to a solution of acetyl chloride (67.0 mL) in ethanol. The reaction mixture is refluxed overnight, cooled, and filtered to remove solids. The resultant filtrate is concentrated in vacuo to obtain a brown semi-solid. A mixture of the semi-solid in diethyl ether is stirred for two hours and filtered to obtain a solid. The solid is washed with diethyl ether and air-dried to give the title product as yellow crystals (1.04 g, mp 91-92° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140270
Source datasetuspto-grants-2000_10
ORD IDord-9759031908084c91be015c2d2538d766
Source noteuspto-grants-2000_10