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HRID 1068387作成日:2026年10月25日

Thionyl Chloride → 5-Chloro-N-hydroxy-N-(1-methylethyl)-3-(trimethylsilyl)-2-thiophenecarboxamide

https://huagongshe.com/reaction/1068387

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物N-Isopropylhydroxylamine HydrochlorideHCID 170873—
反応物Sodium BicarbonateHCID 516892—
反応物5-Chloro-3-(trimethylsilyl)-2-thiophenecarboxylic acidHCID 18630239—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物5-Chloro-N-hydroxy-N-(1-methylethyl)-3-(trimethylsilyl)-2-thiophenecarboxamideHCID 12039976—
生成物5-Chloro-3-(trimethylsilyl)-2-thiophenecarboxylic acid chlorideHCID 54024836—

反応手順

5-Chloro-3-(trimethylsilyl)-2-thiophenecarboxylic acid chloride was prepared by the reaction of 1 g 5-chloro-3-(trimethylsilyl)-2-thiophenecarboxylic acid (prepared as in Example 263) and 6 mL thionyl chloride, using the procedure of step a in Example 248. This product was dissolved in CH2Cl2 at 0° C. and added to a mixture of N-isopropylhydroxylamine hydrochloride (0.55 g, 5 mmol) and 4 g NaHCO3 in 20 mL CH2Cl2 and 20 mL water. The resulting reaction mixture was stirred at RT for additional 3 h. The organic layer was separated, washed with brine, dried and concentrated. The residue was purified by flash chromatography with 8% ethyl acetate/hexane to give 80 mg of the title compound. m.p. 146-150° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06248894B1
出典データセットuspto-grants-2001_06
ORD IDord-a639ace219484057922d5c0cff880b3e
出典メモuspto-grants-2001_06