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HRID 406004作成日:2026年10月25日

(3-Benzyloxy-phenoxy)-tert-butyl-dimethyl-silane → 3-(Tert-butyldimethylsilyl)oxy-1-cyclohexanol

https://huagongshe.com/reaction/406004

反応式

関与物質

役割名称HCID仕込み量
反応物(3-Benzyloxy-phenoxy)-tert-butyl-dimethyl-silaneHCID 58421755—
溶媒EthanolHCID 702—
生成物3-(Tert-butyldimethylsilyl)oxy-1-cyclohexanolHCID 557077—

反応手順

A mixture of 37.6 g (3-benzyloxy-phenoxy)-tert-butyl-dimethyl-silane and 3.8 g of Nishimura's catalyst in 200 ml of ethanol was hydrogenated at rt under 50 psi for 6 hours. The reaction mixture was filtered and the filtrate concentrated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754079B2
出典データセットuspto-grants-2014_06
ORD IDord-733f331f4f134e8484831a22c5f587cc
出典メモuspto-grants-2014_06