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HRID 1860504作成日:2026年10月25日

tert-Butyldimethylsilyl chloride → 1-Benzyl-3-(R)-(t-butyldimethylsilyloxymethyl)-4-(S)-phenylpyrrolidine

https://huagongshe.com/reaction/1860504

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物DiisopropylethylamineHCID 81531—
反応物((3R,4S)-1-Benzyl-4-phenylpyrrolidin-3-YL)methanolHCID 21341047—
溶媒DichloromethaneHCID 6344—
生成物1-Benzyl-3-(R)-(t-butyldimethylsilyloxymethyl)-4-(S)-phenylpyrrolidineHCID 21341048—

反応手順

A solution of 82.0 g (0.31 mol) of 1-benzyl-3-(R)-hydroxymethyl-4-(S)-phenyl pyrrolidine (from Step C) and 46.5 g (0.36 mol) of N,N-diisopropylethylamine in 1 L of CH2Cl2 was treated with 54.2 g (0.36 mol) of t-butyldimethylsilyl chloride and the resulting mixture was stirred at rt for 20 h. The reaction was quenched with 750 mL of sat'd NaHCO3 and the layers were separated. The organic layer was combined with 150 g of silica gel and aged for 45 min. The mixture was filtered and the filtrate was concentrated to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06531484B2
出典データセットuspto-grants-2003_03
ORD IDord-ac8cc2ceae1949a98ed744a434070162
出典メモuspto-grants-2003_03