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HRID 340216作成日:2026年10月26日

3-Chloro-5-(trifluoromethyl)picolinaldehyde oxime → 3-Chloro-5-(trifluoromethyl)pyridine-2-carbonitrile

https://huagongshe.com/reaction/340216

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-5-(trifluoromethyl)picolinaldehyde oximeHCID 718249—
反応物Methyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物3-Chloro-5-(trifluoromethyl)pyridine-2-carbonitrileHCID 1473374—

反応手順

A solution of 3-chloro-5-(trifluoromethyl)picolinaldehyde oxime (1.0 eq.) and Burgess reagent (1.5 eq.) in tetrahydrofuran (0.5 M) was heated to 65° C. and stirred for 1 hour. The reaction was cooled to room temperature and diluted with ethyl acetate and water. The organic layer was washed with water, brine, dried over anhydrous MgSO4, and concentrated en vacuo to give a solid that was carried onto the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895577B2
出典データセットuspto-grants-2014_11
ORD IDord-60b799d726c742ca8d4da0ea1566b81f
出典メモuspto-grants-2014_11