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HRID 24708作成日:2026年10月23日

Imidazole → 3,5-Dimethoxybenzyl tert-butyldiphenylsilyl ether

https://huagongshe.com/ja/reaction/24708

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物3,5-Dimethoxybenzyl alcoholHCID 69718—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
溶媒DimethylformamideHCID 6228—
生成物3,5-Dimethoxybenzyl tert-butyldiphenylsilyl etherHCID 2257188387.9%

反応手順

A mixture of 3,5-dimethoxybenzyl alcohol (4.0 g), tert-butyl-diphenylsilyl chloride (6.54 g) and imidazole (3.28 g) in DMF (60 mL) was stirred at room temperature for 24 h. DMF was evaporated and the residue was purified by column chromatography (silica gel; eluent: hexane to hexane/EtOAc 20% ) to yield 8.5 g of 3,5-dimethoxybenzyl tert-butyldiphenylsilyl ether. ESMS: m/z 407 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855843B2
出典データセットuspto-grants-2005_02
ORD IDord-5a5ba54c17ac44b8bce09720bb95188c
出典メモuspto-grants-2005_02