戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1156670作成日:2026年10月25日

1-(3,4-Dihydroxyphenyl)-2-((1,1-dimethylethyl)amino)ethan-1-one hydrochloride → 4-Chlorotoluene

https://huagongshe.com/reaction/1156670

反応式

関与物質

役割名称HCID仕込み量
反応物1-(3,4-Dihydroxyphenyl)-2-((1,1-dimethylethyl)amino)ethan-1-one hydrochlorideHCID 3015704—
反応物Phenolate SodiumHCID 4445035—
反応物Sodium MethoxideHCID 10942334—
溶媒DimethylformamideHCID 6228—
生成物4-ChlorotolueneHCID 7810—
生成物3-Hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketoneHCID 54189973—

反応手順

Following a procedure similar to that described in Example 58A above, 13 g. of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride was reacted with 8.1 g. of sodium methoxide in 200 ml. of N,N-dimethylformamide, and the resulting sodium phenolate was interacted with 8.5 g. of p-toluyl chloride to yield 3-hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone. This base was converted to the methanesulfonate by treatment, in 200 ml. of warm N,N-dimethylformamide, with methanesulfonic acid. The 3-hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone methanesulfonate thus obtained was a white crystalline solid which weighed 12 g. and melted at 265° C. (dec.)(uncorr.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04336400
出典データセットuspto-grants-1982_06
ORD IDord-58ae942cccc4450a970952def72c33a8
出典メモuspto-grants-1982_06