HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635591Generated: October 31, 2026
Resorcinol → 2,4-Bis(4-tert-butylphenyl)-6-(2,4-dihydroxyphenyl)-1,3,5-triazine
https://huagongshe.com/reaction/1635591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Resorcinol | HCID 5054 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2,4-Bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine (This product is only available in Japan.) | HCID 22475991 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 2,4-Bis(4-tert-butylphenyl)-6-(2,4-dihydroxyphenyl)-1,3,5-triazine | HCID 135804504 | 97.2% |
Reaction Steps
To a 2-neck flask equipped with a reflux condenser, an argon inlet, a magnetic stirring bar and a glass stopper was introduced 3.79 g of 2,4-bis(4-tert-butylphenyl)-6-chloro-1,3,5-triazine of example 1. To it was added 30 mL of chlorobenzene, 1.21 g of resorcinol and 2 g of aluminum chloride at room temperature. The reaction mixture was heated at 85° C. for 6 hr. The heating was discontinued and the reaction was allowed to cool to room temperature. To it was then added 5% ice-cold aq. HCl, and the mixture concentrated under reduced pressure. The residue was washed with water and dried to give 4.4 g of a product characterized to be 2,4-bis(4-tert-butylphenyl)-6-(2,4-dibydroxyphenyl)-1,3,5-triazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06509399B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-43ce290fb6d34381a56fe5f58a794a5b |
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| Source note | uspto-grants-2003_01 |
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