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HRID 28331作成日:2026年10月23日

Tert-Butyl nitrite → 5-[4-(2,2,6,6-Tetramethylpiperidin-1-yloxy)-phenyl]-2-(2-hydroxy-3-alpha-cumyl-5-tert-octylphenyl)-2H-benzotriazole

https://huagongshe.com/ja/reaction/28331

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-Butyl nitriteHCID 10906—
反応物2,2,6,6-Tetramethylpiperidin-1-olHCID 549976—
反応物5-(4-aminophenyl)-2-(2-hydroxy-3-alpha-cumyl-5-tert-octylphenyl)-2H-benzotriazoleHCID 22595033—
溶媒PyridineHCID 1049—
生成物5-[4-(2,2,6,6-Tetramethylpiperidin-1-yloxy)-phenyl]-2-(2-hydroxy-3-alpha-cumyl-5-tert-octylphenyl)-2H-benzotriazoleHCID 1014648887.3%

反応手順

The title compound is prepared reacting 0.59 g (3.75 mmol) of 1-oxyl-2,2,6,6-tetra-methylpiperidine, 1.0 g (10 mmol) of tert-butyl nitrite, 2.3 mg (0.0037 mmol) of (S,S)-(+)-N,N-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II), 120 mL of pyridine and 24.0 g (75 mmol) of 5-(4-aminophenyl)-2-(2-hydroxy-3-α-cumyl-5-tert-octylphenyl)-2H-benzotriazole, prepared in Example 17, in 10 mL of pyridine at 70° C. The crude product obtained is purified by vacuum flash chromatography (2% ethyl acetate/heptane) to give 2.20 g of the title compound as a colorless oil in 87.3% yield. M/S [M+1] 673

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419513B2
出典データセットuspto-grants-2008_09
ORD IDord-db1f92df2b384e879f1959edf9e78cfc
出典メモuspto-grants-2008_09