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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419711Generated: November 1, 2026

Ethyl Acetate → 7-Amino-4-chloro-6-fluoro-2-methylbenzothiazole

https://huagongshe.com/reaction/1419711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-Chloro-6-fluoro-2-methyl-7-nitrobenzothiazoleHCID 53704105—
CatalystIronHCID 23925—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product7-Amino-4-chloro-6-fluoro-2-methylbenzothiazoleHCID 53709923—

Reaction Conditions

Temperature80 °C

Reaction Steps

6 g of iron powder were added to a suspension of 8 g (32 mmol) of 4-chloro-6-fluoro-2-methyl-7-nitrobenzothiazole in 100 ml of water and 9 ml of concentrated hydrochloric acid, which suspension had been heated to 80° C., after which the mixture was refluxed for 3 hours. 200 ml of ethyl acetate were then added to the reaction mixture. The solid was filtered off. The remaining organic phase was washed with water, dried over magnesium sulfate and finally evaporated down. Yield: 4.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05888940
Source datasetuspto-grants-1999_03
ORD IDord-37de1006222e41ceac0e5112e086f55f
Source noteuspto-grants-1999_03