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HRID 1497713作成日:2026年10月25日
(2-Amino-5-bromophenyl)(4-chlorophenyl)methanone → 2-Methyl-propane-2-sulfinic acid (2-amino-5-bromo-phenyl)-(4-chloro-phenyl)-methyleneamide
https://huagongshe.com/reaction/1497713
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (2-Amino-5-bromophenyl)(4-chlorophenyl)methanone | HCID 182477 | — |
| 反応物 | Tert-Butanesulfinamide | HCID 3382465 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-Methyl-propane-2-sulfinic acid (2-amino-5-bromo-phenyl)-(4-chloro-phenyl)-methyleneamide | HCID 123486054 | — |
反応手順
To a solution of (2-Amino-5-bromo-phenyl)-(4-chloro-phenyl)-methanone (13.87 g, 0.05 mol) in THF (200 mL) is added 2-Methyl-propane-2-sulfinic acid amide (6.5 g, 0.05 mol) and Ti(OEt)4 (20.5 g, 0.09 mol).The stirred mixture is refluxed at 80° C. The mixture is quenched with H2O, filtered. THF is removed, extracted with ethyl acetate, dried over NaSO4 and concentrated then purified by silica gel. This produces the desired compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09199988B2 |
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| 出典データセット | uspto-grants-2015_12 |
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| ORD ID | ord-b1e1fe71f526430e872375e4ddd15dbb |
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| 出典メモ | uspto-grants-2015_12 |
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