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HRID 1774作成日:2026年10月24日

2-Aminobenzophenone → 2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenone

https://huagongshe.com/ja/reaction/1774

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminobenzophenoneHCID 76080—
反応物Sodium BicarbonateHCID 516892—
溶媒Ethyl AcetateHCID 8857—
生成物2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenoneHCID 53932370—

反応手順

A mixture of 4.9 g of 5-oxotetrahydrofuran-2-carboxylic acid and 5.5 ml of thionyl chloride was subjected to reflux for 2 hours. Thionyl chloride was then distilled off under reduced pressure to leave 5-oxotetrahydrofuran-2-carbonyl chloride. This product was mixed with 5.0 g of 2-aminobenzophenone, 200 ml of ethyl acetate and 200 ml of a saturated aqueous solution of sodium hydrogencarbonate, which was stirred for one hour at room temperature. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-(5-oxotetrahydrofuran-2-carbonyl)aminobenzophenone (6.5 g) as needles, m.p. 100° C.-102° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726306
出典データセットuspto-grants-1998_03
ORD IDord-947d3e4afae94a0b8dd4f97535b58d90
出典メモuspto-grants-1998_03