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HRID 1450311作成日:2026年10月27日

Imidazole → (Dimethoxyphosphinyl)[[(1,1-dimethylethyl)dimethylsilyl]oxy]acetic acid (4-nitrophenyl)methyl ester

https://huagongshe.com/reaction/1450311

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物DimethylformamideHCID 6228—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Acetic acid, (dimethoxyphosphinyl)hydroxy-, (4-nitrophenyl)methyl esterHCID 10064522—
溶媒Diethylether ethylacetateHCID 21584169—
生成物(Dimethoxyphosphinyl)[[(1,1-dimethylethyl)dimethylsilyl]oxy]acetic acid (4-nitrophenyl)methyl esterHCID 9932571—

反応手順

To a mixture of 3.48 g of product from Example 97 and 12 ml of dimethylformamide is added 1.86 g of t-butyldimethylsilyl chloride and 1.86 g of imidazole. After stirring the reaction at room temperature for 2 hours, the mixture is diluted with ethyl acetate/diethyl ether, washed 5 times with water, once with saturated sodium bicarbonate and once with saturated sodium chloride. The organic layer is dried, filtered and concentrated in vacuo to give 3.90 g of the desired silylated product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05602118
出典データセットuspto-grants-1997_02
ORD IDord-f2ade3ebbf2c4c00a248280dd5841099
出典メモuspto-grants-1997_02