HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23356Generated: October 29, 2026
Cyclohexylamine → n-Cyclohexyl-5-(4-nitrophenyl)-1,3-thiazol-2-amine
https://huagongshe.com/reaction/23356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 2-Bromo-2-(4-nitrophenyl)acetaldehyde | HCID 20188849 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | n-Cyclohexyl-5-(4-nitrophenyl)-1,3-thiazol-2-amine | HCID 12066444 | — |
Reaction Steps
A solution of bromo(4-nitrophenyl)acetaldehyde and potassium thiocyanate (1.2 equivalents) in methanol is stirred at room temperature for 1 hour. The cyclohexylamine (1,05 equivalents) is added drop-wise and the mixture is heated under reflux until completion of the reaction (5-12 hours). After cooling to 0° C. the precipitate is filtered off and washed with water. The crude material is purified by usual silica gel chromatography to give the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852720B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-14089d6065474121a1b9c499e0722165 |
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| Source note | uspto-grants-2005_02 |
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