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HRID 352835作成日:2026年10月26日

4-Methylmorpholine → 4-Chloro-2-methoxybenzaldehyde

https://huagongshe.com/reaction/352835

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物4 Chloro-2-methoxybenzyl alcoholHCID 3549393—
触媒HCID 178419074HCID 178419074—
溶媒DichloromethaneHCID 6344—
生成物4-Chloro-2-methoxybenzaldehydeHCID 13865115—

反応手順

In methylene chloride (80 ml) was dissolved (4-chloro-2-methoxyphenyl)methanol (3.69 g). Under ice cooling, molecular sieve 4A (4.57 g), N-methylmorpholine (2.81 g) and tetra-n-propylammonium perruthenate (420 mg) were added to the resulting solution, followed by stirring at room temperature for 2.5 hours. The reaction mixture was distilled under reduced pressure. The residue was subjected to chromatography on a silica gel column (hexane:ethyl acetate=9:1), whereby the title compound (3.07 g) was obtained as pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747023B1
出典データセットuspto-grants-2004_06
ORD IDord-ad5fea9e0b5f4ceb8a3ddf1d9c72e567
出典メモuspto-grants-2004_06