HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287220Generated: October 31, 2026
Ammonium Hydroxide → 2-Amino-5-Nitrothiazole
https://huagongshe.com/reaction/2287220
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethenamine, N,N-dimethyl-2-nitro- | HCID 518458 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-Nitrothiazole | HCID 8486 | 62% |
Reaction Steps
To a stirred mixture of 3.5 g of N,N-dimethyl-2-nitroetheneamine in 25 ml of acetic acid cooled to 17° C. was added 4.8 g bromine at such a rate the reaction temperature did not exceed 25° C. During bromination an orange solid was formed. After stirring the resulting slurry for 10 minutes, 3.0 g thiourea was added and the reaction mixture exothermed to 32° C. A yellow solid formed. The mixture was stirred for 1 hour and then was diluted with 25 ml of water. This mixture and an approximately equal volume of 29% ammonium hydroxide were added simultaneously to 25 ml of acetic acid at such rates that the pH remained between 4 and 5 and the temperature did not exceed 30° C. After all of the reaction mixture had been added the pH was adjusted to 7 with 29% ammonium hydroxide. The product was then filtered off, washed with water and dried to give 2.7 g (62% yield, 92.9% assay) of 2-amino-5-nitrothiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04269985 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-7a69aba060294d87ae31f76ae80ebd95 |
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| Source note | uspto-grants-1981_05 |
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