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HRID 732661作成日:2026年10月26日

tert-Butyldimethylsilyl chloride → 1-Benzyl-3-t-butyldimethylsilyloxymethylpyrrolidine

https://huagongshe.com/reaction/732661

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(1-Benzylpyrrolidin-3-yl)methanolHCID 5176654—
溶媒ChloroformHCID 6212—
生成物1-Benzyl-3-t-butyldimethylsilyloxymethylpyrrolidineHCID 19914927—

反応手順

Diisopropylethylamine and tert-butyldimethyl-chlorosilane were added in that order to a chloroform solution of (1-benzylpyrrolidin-3-yl)methanol and stirred at room temperature for 5Hours. Thereafter, its work-up and purification were carried out in the standard method to obtain 1-benzyl-3-({[tert-butyl(dimethyl)silyl]oxy}methyl]pyrrolidine. EP: 306.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07585886B2
出典データセットuspto-grants-2009_09
ORD IDord-22633246d1ab409e8e61f01d745b9caa
出典メモuspto-grants-2009_09