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HRID 500024作成日:2026年10月24日

4,4'-Methylenebis[2,6-diethylaniline] → N,N'-di-sec-butyl-4,4'-methylenebis(2,6-diethylbenzeneamine)

https://huagongshe.com/ja/reaction/500024

反応式

関与物質

役割名称HCID仕込み量
反応物4,4'-Methylenebis[2,6-diethylaniline]HCID 83656—
触媒PlatinumHCID 23939—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物N,N'-di-sec-butyl-4,4'-methylenebis(2,6-diethylbenzeneamine)HCID 6678112994%

反応条件

温度95 °C

反応手順

4,4′-Methylenebis(2,6-diethylbenzeneamine) (4.0 g), Pt(S)/C (0.2 g), sulfonated divinylbenzene/styrene copolymer (0.2 g; H ion form, sold as Amberlyst-15 by Rohm and Haas Company, Philadelphia, Pa.), and methyl ethyl ketone (50 g) were charged into a 100 mL metal autoclave at 22° C. The closed autoclave was purged 3 times with 125 psig (9.63×105 Pa) of H2 at 22° C. to remove traces of air. The reaction mixture was then heated at 95° C. under 125 psig (9.63×105 Pa) of H2 for 3 hours (until no further H2 uptake was observed). The product mixture was cooled to 22° C. and degassed. A diluted product sample was analyzed by gas chromatography (GC; 180° C. for 5 minutes at 10° C. per minute rate; final temperature, 270° C.). The GC data (normalization method) showed 100% conversion of 4,4′-methylenebis(2,6-diethylbenzeneamine) and a 94% yield of N,N′-di-sec-butyl-4,4′-methylenebis(2,6-diethylbenzeneamine). NMR analysis (with internal standard) of a neat product sample showed a purity of 94.75%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07767858B2
出典データセットuspto-grants-2010_08
ORD IDord-4429643e88a74e389a00f7372bbf160e
出典メモuspto-grants-2010_08