関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 1-(Methylsulfonyl)-3-nitrobenzene | HCID 76312 | — |
| 溶媒 | Water ethanol | HCID 19096565 | — |
| 生成物 | 3-(Methylsulphonyl)aniline | HCID 428029 | 85.5% |
反応手順
(3-Nitro)phenyl methyl sulphone (prepared as described in Step 1 above) (5.396 g) reduced iron (7.5 g) and ammonium chloride (7.18 g) were mixed together in ethanol/water (2:1) (150 ml) and heated under reflux for 2 hours. The black solution was filtered through `Celite` and the pad washed with ethyl acetate. The solvents were removed under reduced pressure and the residue taken up in ethyl acetate/water. The organic layer was separated and the aqueous layer extracted with 3 further portions of ethyl acetate. The combined organic layers were washed with brine and the solvent removed under reduced pressure to give a dark orange oil (3.9275 g). This was chromatographed on silica gel using ethyl acetate-hexane (45:55 to 50:50) as eluant to give the title compound as an orange oil, yield 3.607 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05856273 |
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| 出典データセット | uspto-grants-1999_01 |
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| ORD ID | ord-468b3da800a94e858c6b6de404755328 |
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| 出典メモ | uspto-grants-1999_01 |
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