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HRID 50413作成日:2026年10月23日

Resorcinol → 1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)-

https://huagongshe.com/ja/reaction/50413

反応式

関与物質

役割名称HCID仕込み量
反応物ResorcinolHCID 5054—
反応物M-XyleneHCID 7929—
反応物Cyanuric chlorideHCID 7954—
反応物1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)-HCID 71059—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒ChlorobenzeneHCID 7964—
生成物1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)-HCID 71059—
生成物2,4,6-Tris(2,4-dimethylphenyl)-1,3,5-triazineHCID 22475988—

反応手順

Cyanuric chloride was allowed to react with 2.05 eq of m-xylene, in the presence of 3 eq of AlCl3 and 0.2 of resorcinol, in chlorobenzene at 5° C. for 0.5 h and then at room temperature for 3 h. The first step (conversion to 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine) was completed in less than 16 h, with more than 98% cyanuric chloride conversion as determined by HPLC analysis. 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine and 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine were formed in an 86:14 ratio; no other products were detected. The reaction mixture was allowed to react with additional resorcinol at 110° C. for 1.5 h. HPLC analysis showed a product mixture of 82% 2-(2,4-dihydroxyphenyl)-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine, 14% 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine, and 2% 2,4,6-tris(2,4-dihydroxyphenyl)-1,3,5-triazine, with only 1.5% unreacted 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710177B2
出典データセットuspto-grants-2004_03
ORD IDord-a98db76593b44ef79acd4d9ab98eb4ff
出典メモuspto-grants-2004_03