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HRID 1776175作成日:2026年10月26日

N-(2-(hydroxymethyl)phenyl)methanesulfonamide → 2-(Methylsulfonamido)benzaldehyde

https://huagongshe.com/reaction/1776175

反応式

関与物質

役割名称HCID仕込み量
反応物N-(2-(hydroxymethyl)phenyl)methanesulfonamideHCID 22955815—
触媒HCID 178418406HCID 178418406—
溶媒DichloromethaneHCID 6344—
生成物2-(Methylsulfonamido)benzaldehydeHCID 11579304—

反応手順

The title compound was synthesized according to the method described in WO 2008/073956 A2. To a solution of N-(2-(hydroxymethyl)phenyl)methanesulfonamide (3.44 g, 17.1 mmol) in anhydrous methylene chloride (68 mL) was added manganese dioxide (85% Aldrich, 17 g) and the mixture was stirred at ambient temperature overnight. Additional manganese dioxide (1.6 g) was added and the mixture stirred at 30° C. for 8 hours. The mixture was filtered through Celite, washing with methylene chloride, and the organic solution concentrated. The crude residue was purified by silica gel column chromatography (40-60% ethyl acetate in hexanes) to give a white solid (2.1 g, 62%). 1H NMR (CDCl3, 300 MHz) δ 10.59 (br s, 1H), 9.91 (s, 1H), 7.75-7.59 (m, 3H) 7.28-7.23 (t, 1H, J=7.5 Hz), 3.12 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09265772B2
出典データセットuspto-grants-2016_02
ORD IDord-0bc6a7ed187344eabab9d5f92a5e1981
出典メモuspto-grants-2016_02