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HRID 434303作成日:2026年10月25日

3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (R)-(+)- → HCID 68809475、化合物

https://huagongshe.com/reaction/434303

反応式

関与物質

役割名称HCID仕込み量
反応物3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (R)-(+)-HCID 178792—
反応物4-(4-Fluorobenzoyl)piperidineHCID 2724440—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 68809475HCID 68809475—

反応手順

To a solution of (4-fluoro-phenyl)-piperidin-4-yl-methanone (3.5 g, 17 mmol) in dry tetrahydrofuran (50 ml) is added (R)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (3.9 g, 17 mmol) and sodium triacetoxyborohydride (5.4 g, 25 mmol), and the reaction mixture stirred for 18 hours at ambient temperature. The reaction mixture is filtered and the solvent evaporated to give a white solid. The solid is taken up in dichloromethane (50 ml) and washed with saturated sodium bicarbonate solution (50 ml), water (2×50 ml) and brine (50 ml). The organic phase is dried over magnesium sulphate and evaporated to afford the product, [MH]+420.9.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06670379B2
出典データセットuspto-grants-2003_12
ORD IDord-bcb2009a4e644e87a58309e501982678
出典メモuspto-grants-2003_12