HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461367Generated: November 2, 2026
Aniline → 2-Anilino-4-chloro-5-nitrothiazole
https://huagongshe.com/reaction/1461367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,4-Dichloro-5-nitro-1,3-thiazole | HCID 13851817 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Anilino-4-chloro-5-nitrothiazole | HCID 15058918 | 94.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05075326 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-c533bd4e6cb14d8aa83c8a3d93dd7d24 |
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| Source note | uspto-grants-1991_12 |
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