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HRID 467520作成日:2026年10月25日

Sodium hydride → Benzyl 3-(2-benzyloxyethoxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/467520

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Benzene, ((2-bromoethoxy)methyl)-HCID 73833—
反応物Benzyl 3-hydroxypyrrolidine-1-carboxylateHCID 560953—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl 3-(2-benzyloxyethoxy)pyrrolidine-1-carboxylateHCID 7092704322.2%

反応条件

温度80 °C

反応手順

A solution of 1.29 g of benzyl 3-hydroxypyrrolidine-1-carboxylate in 80 ml of THF is cooled to 0° C., 0.245 g of 60% NaH in oil is added and then 1.26 g of [(2-bromoethoxy)methyl]benzene and 0.108 g of tetrabutylammonium iodide and it is heated at 80° C. for 3 hours. 0.28 g of NaH and 0.40 g of [(2-bromoethoxy)methyl]benzene are added and it is heated at 80° C. for 2 hours. The reaction mixture is concentrated under vacuum, the residue is extracted with DCM, the organic phase is washed with 0.1M HCl solution, with a saturated solution of NaHCO3, it is dried and the solvent is evaporated under vacuum. The product thus obtained is purified by preparative HPLC and 0.46 g of the expected compound is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08623862B2
出典データセットuspto-grants-2014_01
ORD IDord-31c6ebefc897422a9c8ff8c9e97cc707
出典メモuspto-grants-2014_01