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HRID 261741作成日:2026年10月27日

Phenol, 2,6-bis(1,1-dimethylethyl)-4-nitroso- → 4-Amino-2,6-di-tert-butylphenol

https://huagongshe.com/reaction/261741

反応式

関与物質

役割名称HCID仕込み量
反応物Phenol, 2,6-bis(1,1-dimethylethyl)-4-nitroso-HCID 70383—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物4-Amino-2,6-di-tert-butylphenolHCID 314220—

反応手順

2,6-di tert.butyl-4-aminophenol was prepared by hydrogenating a mixture of 23.5 grams of 2,6-di tert.butyl-4-nitrosophenol, 2 grams of 5% Palladium on carbon, and 200 milliliters of absolute ethanol in a Parr Pressure Reaction Apparatus. The reduction was accomplished in 1 hour at a maximum hydrogen pressure of 50 psi and a maximum temperature of 50° C. The resulting solution of 2,6-di tert.butyl-4-aminophenol was removed from the Pressure Apparatus and filtered to remove the catalyst.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04152319
出典データセットuspto-grants-1979_05
ORD IDord-02082f82b5dc4dbcbea7f30a89d500c5
出典メモuspto-grants-1979_05