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HRID 620704作成日:2026年10月24日
Benzamide, N-(4-amino-5-chloro-2-hydroxyphenyl)- → 2-Benzamido-4-chloro-5-[2-(p-nitrophenoxy]-myristamido]-phenol
https://huagongshe.com/ja/reaction/620704
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzamide, N-(4-amino-5-chloro-2-hydroxyphenyl)- | HCID 78779 | — |
| 反応物 | 2-(4-nitrophenoxy)tetradecanoyl Chloride | HCID 2735105 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-Benzamido-4-chloro-5-[2-(p-nitrophenoxy]-myristamido]-phenol | HCID 14122421 | — |
反応手順
An amount of 843 g (2.1 mol) of 2-(p-nitrophenoxy]-myristoyl chloride is added dropwise in 60 min to a cooled (0°-5° C.) solution of 525 g (2 mol) of 2-benzamido-4-chloro-5-aminophenol in 6 l of tetrahydrofuran and 220 ml of quninoline. The temperature of the reaction mixture is kept below 10° C. The precipitate of quinoline hydrochloride is filtered off. The filtrate is concentrated by evaporation. The residual oil is poured out in 5 l of hot (50° C.) acetonitrile. Upon cooling to 5° C. a precipitate forms, whch is filtered, dried, and recrystallized from boiling isopropyl ether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04822729 |
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| 出典データセット | uspto-grants-1989_04 |
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| ORD ID | ord-67c0bc5e2896474aa323a70f8471ceea |
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| 出典メモ | uspto-grants-1989_04 |
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