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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461367Generated: November 1, 2026

Aniline → 2-Anilino-4-chloro-5-nitrothiazole

https://huagongshe.com/reaction/1461367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantSodium BicarbonateHCID 516892—
Reactant2,4-Dichloro-5-nitro-1,3-thiazoleHCID 13851817—
SolventAcetonitrileHCID 6342—
Product2-Anilino-4-chloro-5-nitrothiazoleHCID 1505891894.4%

Reaction Steps

252 g (3.0 mols) of sodium bicarbonate are added to a solution of 360 g (1.8 mols) of 2,4-dichloro-5-nitrothiazole in 1.5 l of acetonitrile. A mixture of 139.5 g (1.5 mols) of aniline and 1,500 ml of acetonitrile is then added dropwise at -10° C. to -15° C. in the course of about 4.5 hours and the mixture is subsequently stirred at the same temperature for a further 4 hours. It is then stirred into 15 l of ice-water and the precipitate is filtered off, washed with water and dried. To remove excess 2,4-dichloro-5-nitrothiazole, the product is stirred into 2.4 l of petroleum ether at room temperature, filtered off, washed with petroleum ether and dried. 361.7 g (94.4% of theory) of 2-anilino-4-chloro-5-nitrothiazole of melting point 186° C. to 187° C. (decomposition) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075326
Source datasetuspto-grants-1991_12
ORD IDord-c533bd4e6cb14d8aa83c8a3d93dd7d24
Source noteuspto-grants-1991_12