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HRID 393911作成日:2026年10月26日

4-Nitrophenol → 4-Nitrophenyl 2-chloro-4-(methylsulfonyl)benzoate

https://huagongshe.com/reaction/393911

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrophenolHCID 980—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物2-Chloro-4-(methylsulfonyl)benzoic acidHCID 735863—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物4-Nitrophenyl 2-chloro-4-(methylsulfonyl)benzoateHCID 22648324—

反応手順

A 200-mL round bottom flask was fitted with thermometer, magnetic stirrer, and reflux condenser with nitrogen bypass. The flask was charged with 0.94 g (4 mmol) of 2-chloro-4-(methylsulfonyl)benzoic acid, 2 drops of DMF, and 20 mL of dichloromethane. Oxalyl chloride (0.56 g, 4.4 mmol) was added dropwise and the mixture was stirred for 1 hr. A solution consisting of 0.62 g (4 mmol) of 4-nitrophenol, 0.44 g (4.4 mmol) of triethylamine and 5 mL of dichloromethane was added slowly. The mixture was stirred for 1 hr, diluted with 100 mL of dichloromethane, washed twice with 100 mL portions of dilute aqueous sodium bicarbonate, once with water, dried over magnesium sulfate, filtered, and volatiles removed under reduced pressure to give the title product as 1.30 g of off-white solid, m.p. 123-125° C. 1H NMR (CDCl3): δ 3.14 (s, 3), 7.48 (m, 2), 8.00 (m, 1), 8.14 (m, 1), 8.21 (m, 1), 8.36 (m, 2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06809206B2
出典データセットuspto-grants-2004_10
ORD IDord-2cbb3bcbb91f4deead7c783c0e3e4ff3
出典メモuspto-grants-2004_10