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HRID 423360作成日:2026年10月25日

Iodoform → 4-Carboxy-2-iodobenzotrifluoride, 3-Iodo-alpha,alpha,alpha-trifluoro-p-toluic acid

https://huagongshe.com/reaction/423360

反応式

関与物質

役割名称HCID仕込み量
反応物IodoformHCID 6374—
反応物Butyl nitriteHCID 10996—
反応物3-Amino-4-(trifluoromethyl)benzoic acidHCID 642651—
溶媒TetrahydrofuranHCID 8028—
生成物4-Carboxy-2-iodobenzotrifluoride, 3-Iodo-alpha,alpha,alpha-trifluoro-p-toluic acidHCID 59318424—

反応条件

温度80 °C

反応手順

3-Amino-4-(trifluoromethyl)benzoic acid (commercially available) (6.5 g, 31.7 mmol) and triiodomethane (37.4 g, 95.1 mmol) were dissolved in THF (300 ml). The reaction mixture was heated to 80° C. and then butyl nitrite (5.56 ml, 47.6 mmol) was added slowly at this temperature. Heating was continued at this temperature for 4 hours and then the reaction was concentrated in vacuo to give the crude product. Purification by column chromatography (hexane to 30% EtOAc in hexane). This material was combined with another batch from a similar reaction performed on 2 g of 3-amino-4-(trifluoromethyl)benzoic acid. The combined material was purified by preparative HPLC to give the title compound (6.1 g). MS C8H4F3IO2 requires 316; found 315 (M−H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101775B2
出典データセットuspto-grants-2012_01
ORD IDord-8c22aa50f5d6404d9219efda24c2f897
出典メモuspto-grants-2012_01