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HRID 412162作成日:2026年10月23日

Triethylamine → 2.5-Di-[(methanesulfonyl)oxy]benzaldehyde

https://huagongshe.com/ja/reaction/412162

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物2,5-DihydroxybenzaldehydeHCID 70949—
溶媒DichloromethaneHCID 6344—
生成物2.5-Di-[(methanesulfonyl)oxy]benzaldehydeHCID 18536186—

反応手順

To a solution of 2,5-dihydroxybenzaldehyde (8.22 g, 59.5 mmol) in 100 mL of dichloromethane at 0° C. was added triethylamine (24.8 mL, 178 mmol), followed by dropwise addition of methanesulfonyl chloride (10.1 mL, 130 mmol). After 30 minutes, the solution was concentrated in vacuo, then partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The product was isolated as a brown oil which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06562823B1
出典データセットuspto-grants-2003_05
ORD IDord-5623e8b1669c443d8e97930d5d019eb5
出典メモuspto-grants-2003_05