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HRID 480035作成日:2026年10月26日

Triethylamine → 2-(Tert-butyldimethylsilyloxy)furan

https://huagongshe.com/reaction/480035

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2(5H)-FuranoneHCID 10341—
反応物tert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
溶媒DichloromethaneHCID 6344—
生成物2-(Tert-butyldimethylsilyloxy)furanHCID 10867303—

反応手順

To a freshly distilled solution of 2(5H)-furanone (2.86 g, 34 mmol) in dichloromethane (20 ml), distilled triethylamine (6.6 ml. 47.4 mmol) is added under argon at 0° C. and then rapidly followed by tert-butyldimehylsilyltrifluoromethane sulfonate (8.6 ml, 37.3 mmol) The reaction mixture is allowed to return to room temperature and the stirring is maintained for two hours. The solvent is then removed under reduced pressure and the oily residue is purified by flash chromatography on silica gel (ethyl acetate-heptane, 1:9) in order to thus obtain compound 10 (Z=O) in the form of a slightly colored oil (5.3 g, 79%). The spectroscopic data for this compound (1H and 13C NMR) are identical to those described in the literature (G. Rassu, Z. Zanardi, L. Battistini, E. Gaetani, G. Casiraghi, J. Med. Chem ., 1997, 40, 168).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06649626B1
出典データセットuspto-grants-2003_11
ORD IDord-f42274949c0f4f5a89dca6573bc1fbee
出典メモuspto-grants-2003_11