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HRID 58606作成日:2026年10月26日

Oxalyl chloride → Ethyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/reaction/58606

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物3-(Trifluoromethyl)benzeneacetic acidHCID 67695—
反応物DiisopropylethylamineHCID 81531—
反応物Ethyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
溶媒PyridineHCID 1049—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylateHCID 668321614%

反応手順

This compound was prepared according to general method 2 with (step I) 2-(3-(trifluoromethyl)phenyl)acetic acid (0.773 g; 3.78 mmol) and oxalyl chloride (0.352 mL; 4.16 mmol) in dichloromethane (12 mL) with few drops of DMF and (step II) ethyl 2-amino-2-(hydroxyimino)acetate (0.5 g; 3.78 mmol) and N,N diisopropylethylamine (1.05 mL; 6.06 mmol) in dichloromethane (6 mL) and (step III) pyridine (18 mL). The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.040 g (4%) of ethyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylate as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434722B2
出典データセットuspto-grants-2016_09
ORD IDord-b52d720bc7124155aa8989ca832bdea6
出典メモuspto-grants-2016_09