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HRID 23817作成日:2026年10月26日
Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)- → 2,3,5-Trichloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamide
https://huagongshe.com/reaction/23817
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)- | HCID 11037 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | Hydrochloride methanol | HCID 21893726 | — |
| 反応物 | 2,3,5-trichloro-N-(2-hydroxyimino-ethyl)-benzamide | HCID 73987901 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2,3,5-Trichloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamide | HCID 22590599 | 32% |
反応手順
To a solution of 2,3,5-trichloro-N-(2-hydroxyimino-ethyl)-benzamide (0.85 g, 3.0 mmol ) in MeOH (50 mL) under an argon atmosphere at 0° C. was added methyl orange (trace) followed by a saturated solution of MeOH/HCl until a persistent red color was observed. Sodium cyanoborohydride (0.23 g, 3.65 mmol) was dissolved in MeOH (5 mL) was added sequentially with saturated MeOH/HCl over 0.5 h. The reaction mixture was stirred an additional 1 h and the MeOH was removed in vacuo. The residue was basidified with 10% NaOH and extracted (4×25 mL) with dichloromethane/MeOH (9:1). The combined organic extracts were washed with brine, were dried (NaHCO3) and were concentrated. The residue was diluted with ether/MeOH (9:1) and the precipitate was collected to provide the title compound (0.27 g, 32%) as a white solid. ESMS: M+H=283.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06852882B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-90150c212a0d4468a4c4d3217e1434c3 |
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| 出典メモ | uspto-grants-2005_02 |
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