関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfamic Acid | HCID 5987 | — |
| 反応物 | N-Ethyl-N-benzylaniline | HCID 7098 | — |
| 反応物 | Nitrosylsulfuric acid | HCID 82157 | — |
| 反応物 | 3-Amino-4-chlorobenzenesulphonyl fluoride | HCID 97383 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Acetic propionic acid | HCID 131720610 | — |
| 生成物 | 4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl aniline | HCID 53969731 | — |
反応手順
3-Amino-4-chloro benzene sulphonyl fluoride (2 parts) was stirred in acetic/propionic acid 86/14 vol/vol (25 parts) and cooled to 0°-5° C. Nitrosyl sulphuric acid solution (3.8 parts) was added dropwise at 0°-5° C. and stirred under these conditions for 2 hours. The diazo solution was then added to a mixture of N-ethyl-N-benzyl aniline (2.7 parts), methanol (100 parts) and sulphamic acid (1 part) stirring at 0°-5° C. After stirring under these conditions for 30 mins, ice/water (100 parts) was added and the mixture stirred for a further 1 hour. The product was isolated by filtration, washed with water and pulled dry. The damp solid was then slurried in methanol (100 parts) and refiltered. Dried at 50° C. to yield 4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl aniline (2.3 parts).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05739299 |
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| 出典データセット | uspto-grants-1998_04 |
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| ORD ID | ord-559d64b2333f46a0803664a50d614084 |
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| 出典メモ | uspto-grants-1998_04 |
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