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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413867Generated: October 26, 2026

3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone → 5-amino-3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazolone

https://huagongshe.com/reaction/2413867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazoloneHCID 14014244—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product5-amino-3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazoloneHCID 1401424571.7%

Reaction Steps

Electrolytic iron powder (0.29 g) was suspended in 5% acetic acid (2 ml), and a solution of 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone (0.31 g) in acetic acid (1 ml) and ethyl acetate (1 ml) was dropwise added thereto while heating. The resultant mixture was heated under reflux for 3 hours. The reaction mixture was subjected to filtration with celite, and the filtrate was extracted with ethyl acetate. The extract was washed with water and sodium bicarbonate solution, dried and concentrated to give 0.20 g of 5-amino-3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazolone. m.p., 172.5°-173.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04720297
Source datasetuspto-grants-1988_01
ORD IDord-7a49f3b3f702425d888959464e3b06dc
Source noteuspto-grants-1988_01