HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111085Generated: October 25, 2026
4-Methylbenzaldehyde → 5-Nitro-2-p-tolylbenzo[d]thiazole
https://huagongshe.com/reaction/1111085
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | 2-Amino-4-nitrobenzenethiol | HCID 6336400 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-Nitro-2-p-tolylbenzo[d]thiazole | HCID 22153305 | — |
Reaction Steps
To a stirred solution of 153.2 g (0.9 mole) of 2-amino-4-nitrothiophenol in pyridine is added 108.1 g (0.9 mole) of 4-tolualdehyde, and the reaction is heated at 100° C. until the starting materials are consumed. After cooling to room temperature, the mixture is acidified with cold 2N HCl, and the intermediate benzthiazoline is collected by filtration. The benzthiazoline is dissolved in methanol, then ferric chloride is added, and the solution is warmed at 40° C. for about 2 hours until oxidation to the benzthiazole is complete. The product is recrystallized from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04978476 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-ef8be7f63e6b4f77b92af929e1eabe0a |
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| Source note | uspto-grants-1990_12 |
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