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HRID 443701作成日:2026年10月25日

m-(Trifluoromethyl)benzamide → 5-(alpha,alpha,alpha-Trifluoro-m-Tolyl)-1,3,4-Oxathiazol-2-One

https://huagongshe.com/reaction/443701

反応式

関与物質

役割名称HCID仕込み量
反応物m-(Trifluoromethyl)benzamideHCID 74535—
反応物(Chlorothio)formyl chlorideHCID 75990—
溶媒Ethyl AcetateHCID 8857—
生成物5-(alpha,alpha,alpha-Trifluoro-m-Tolyl)-1,3,4-Oxathiazol-2-OneHCID 1226011086.3%

反応手順

α,α,α-Trifluoro-m-toluamide (82.7 g, 0.437 mol) and chlorocarbonylsulfenyl chloride (86 g, 0.667 mol, 53% excess) were reacted under the conditions of Example 2 for 0.5 hours. The light yellow residue was dissolved in ethyl acetate and cooled to -78°. The white precipitate was filtered and washed with hexane to yield 93.14 g (0.377 mol, 86.2%) of white solid, m.p. 85°-86.5°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04261728
出典データセットuspto-grants-1981_04
ORD IDord-745498c25ccc40d08310b90c6e84aa74
出典メモuspto-grants-1981_04