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HRID 32248作成日:2026年10月24日

[4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)phenyl]methanol → 4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzaldehyde

https://huagongshe.com/ja/reaction/32248

反応式

関与物質

役割名称HCID仕込み量
反応物[4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)phenyl]methanolHCID 23142118—
触媒HCID 178418406HCID 178418406—
溶媒ChloroformHCID 6212—
生成物4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzaldehydeHCID 2314250085.1%

反応手順

A mixture of the crude product of [4-(4-t-butylcyclohexyl)-3-(4-butylpiperazin-1-yl)phenyl]methanol produced in Example (101a) (294 mg), manganese (IV) oxide (1.3 g, 14.95 mmol) and chloroform (15 mL) was refluxed for 40 minutes. The reaction mixture was filtered and insoluble materials were filtered off. The filtrate was concentrated under reduced pressure to give 249 mg of a crude product of the title compound as an ochre oil. This product was directly used without purification for the following reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425554B2
出典データセットuspto-grants-2008_09
ORD IDord-449de0b95d344595ad9297220a8b494d
出典メモuspto-grants-2008_09