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HRID 1049404作成日:2026年10月26日

(3-(((Tert-butyldiphenylsilyl)oxy)methyl)phenyl)methanol → Benzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-

https://huagongshe.com/reaction/1049404

反応式

関与物質

役割名称HCID仕込み量
反応物(3-(((Tert-butyldiphenylsilyl)oxy)methyl)phenyl)methanolHCID 57049439—
触媒HCID 178418406HCID 178418406—
溶媒TetrahydrofuranHCID 8028—
生成物Benzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-HCID 1088327995.5%

反応手順

To a solution of (3-(((tert-butyldiphenylsilyl)oxy)methyl)phenyl)methanol (6.96 g) in THF (37 mL) was added manganese(IV) oxide (8.03 g), and the mixture was stirred at room temperature for 5.5 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (6.61 g) as a pale-yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09382188B2
出典データセットuspto-grants-2016_07
ORD IDord-d468fae0eea74f0eae0320f6c0260089
出典メモuspto-grants-2016_07