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HRID 467187作成日:2026年10月26日

Tazofelone → 5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-2-thioxo-4-thiazolidinone

https://huagongshe.com/reaction/467187

反応式

関与物質

役割名称HCID仕込み量
反応物TazofeloneHCID 68745—
反応物3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
反応物RhodanineHCID 1201546—
反応物5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-2-thioxo-4-thiazolidinoneHCID 3071511—
反応物3,5-Bis (1,1-dimethylethyl)-4-thiazolidinoneHCID 57283997—
反応物[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]-methylene-4-thiazolidinoneHCID 86746307—
溶媒Acetic AcidHCID 176—
生成物5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-2-thioxo-4-thiazolidinoneHCID 9968356—

反応手順

The aryl-substituted rhodanine derivatives of formula I are either known in the art or may be prepared by any of a number of well-known procedures. For example, Teuber et al., Leibigs Ann. Chem., 757 (1978) disclose 5-[[3,5-bis(1,1-dimethylethyl)-4hydroxyphenyl]methylene]-2-thioxo-4-thiazolidinone (referred to in the following discussion as Compound A). The compound is prepared by reacting 3,5-di-tert-butyl-4-hydroxybenzaldehyde with rhodanine at reflux temperature in glacial acetic acid using fused sodium acetate as catalyst. 5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]-methylene-4-thiazolidinone (Compound B), 5-[[3,5-bis-(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-4-thiazolidinone (Compound C) and 5-[[3,5-bis (1,1-dimethylethyl)-4-thiazolidinone (Compound D) can be prepared from Compound A as follows.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05158966
出典データセットuspto-grants-1992_10
ORD IDord-3db86b1154fe427fb5a62c4ece6d84ac
出典メモuspto-grants-1992_10