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HRID 38702作成日:2026年10月24日

Methyl morpholine oxide → 2-Bromo-5-(trifluoromethyl)benzaldehyde

https://huagongshe.com/ja/reaction/38702

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl morpholine oxideHCID 82029—
反応物2-Bromo-5-(trifluoromethyl)benzyl alcoholHCID 2756248—
触媒HCID 178419074HCID 178419074—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物2-Bromo-5-(trifluoromethyl)benzaldehydeHCID 7018047—

反応手順

2-Bromo-5-(trifluoromethyl)benzyl alcohol (2.216 g, 8.69 mmol) and N-methylmorpholine-N-oxide (2.051 g, 17.38 mmol) were combined in CH2Cl2 (44 mL) and MeCN (2.2 mL). Tetrapropylammonium perruthenate (0.311 g, 0.87 mmol) was added, and the reaction was stirred for 20 minutes at room temperature. Once no starting material was seen by analytical tlc, the mixture was concentrated, and the residue was purified by silica gel chromatography to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524748B2
出典データセットuspto-grants-2013_09
ORD IDord-3b24e4b4e1b945c3aacdfacc4a0d6bd9
出典メモuspto-grants-2013_09