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HRID 250199作成日:2026年10月26日

Dimethylformamide → 4-Methoxyindole-3-aldehyde

https://huagongshe.com/reaction/250199

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物4-Methoxy-1H-indoleHCID 138363—
溶媒1,1-DichloroethaneHCID 6365—
生成物4-Methoxyindole-3-aldehydeHCID 14622996.3%

反応手順

A solution of dry DMF (0.75 g) in 50 ml dichloroethane was cooled to 0° C. and placed under nitrogen. Oxalyl chloride (1.03 g) dissolved in dichloroethane (5 ml) was added dropwise with stirring. The solution was stirred until no more bubbling was observed (about 15-20 m). 4-Methoxyindole (1.0 g, 6.7 mmole) was added to the solution as a solid and the reaction mixture was stirred at room temperature for four hours. The reaction was quenched by careful addition of 10% sodium carbonate solution. The two phase mixture was stirred at room temperature for 2 hours. The layers were separated and the aqueous layer was extracted with methylene chloride, and the combined organic extracts were dried and evaporated to dryness. The crude residue was passed through a short silica gel column, eluting with 3:7 ethyl acetate:hexane to 1:1 ethyl acetate:hexane to yield 1.13 g (95%) of 4-methoxy-1H-indole-3-carbaldehyde.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863305B2
出典データセットuspto-grants-2011_01
ORD IDord-49570dac9afd4c6fa553e2c3fbddfdf1
出典メモuspto-grants-2011_01